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Haplogroup N-M231

Haplogroup N (M231) is a Y-chromosome DNA haplogroup defined by the presence of the single-nucleotide polymorphism (SNP) marker M231.[Phylogenetics 1]

Haplogroup N
Possible time of origin36,800 [95% CI 34,300–39,300] years before present (YFull[1])

44,700 or 38,300 ybp depending on mutation rate[2]

41,900 [95% CI 40,175-43,591] ybp[3]
Coalescence age21,700 [95% CI 19,500–23,900] ybp (YFull[1])

25,313 [95% CI 21,722–28,956] ybp[3]
Possible place of originNorthern East Asia[4][5]
AncestorNO
Defining mutationsM231
Highest frequenciesNganassan 58%[3]-94.1%,[6] Yakuts 81.8%[7]-94.6%[8] (Xu 2015), Khakass (Shirinsky District) 90.2%,[9] Siberian Tatars (Zabolotnie Tatars) 89.5%,[10] Ugrians 77.8%[3] (Khanty 64.3%[11]-89.3%,[12] Mansi 76%[12]), Udmurts 77.8%,[3] Khakas 41%[3] – 65%,[11] Komi 33.3%[11]-79.5%,[6] Nenets 75%–92.9%[3] (Tundra Nenets 97.9%,[6] Forest Nenets 98.8%[6]), Vepsians 55%,[3] Finns 42.6% (West)[13] - 70.9% (East)[13] or approx. 54%,[3] Tuvans 27.2–54.5% (Kharkov 2013), Nanai 46.2%[14][15][3] (20% Hezhe in the PRC,[14] 44.6% Nanai in Russia,[3] 83.8% members of the Samar clan in the Gorin area of the Khabarovsk Territory[15]), Karelians 37.1%[16]-53.8%,[13] Arkhangelsk Russians 42.6% (Arkhangelsk 44.3%,[3] Pinega 40.8%[3]), Lithuanian 40.5%[3]-44.5%,[13] Latvian approx. 42% (41.6%,[13] 42.1%,[17] 43.0%[3]), Mari 41.2%,[3] Saami 40%, Chuvash 33.7%[18]-36%,[3] Buryats 34.5% (20.2%,[19] 25.0%,[20] 30.9%,[21] 48.0%[22]), Koryaks 33.3%,[6] Estonian 30.6%[3]-33.9%,[13] Volga Tatars 27.8%,[3] Teleuts 25.0%,[6] Northern Altaians 21.8% (18.0%[11][23]-24.6%[24]), Pskov Russians 22.7%,[3] Bashkirs 17.3%,[3] Sibe 17.1%[14]-18.0%,[25] Mordvins 12.5% (10%[3] – 13.3%[3]), Mongols 11%,[26][21][14][20][27][28] Kalmyks 10.4% (Torguud 3.4%, Derbet 5.1%, Buzava 5.3%, Khoshut 38.2%),[29][28] Manchus 10% (5.8%,[21] 8.1%,[30] 9.1%,[25] 11.6%,[25] 12.5%,[25] 14.3%[14]), Belarusians 9.7%,[3] Central-Southern Russians 9.1% (Tver 13.2%,[31] Kursk 12.5%[31]-13.3%,[3] Belgorod 11.9%,[3] Kostroma 11.8%,[3] Smolensk 7.0%,[3] Voronezh 6.3%,[3] Oryol 5.5%[3]), Ukrainians 9.0%,[3] Southern Altaians 7.1% (4.2%[24]-9.7%[11]), Mulam 7.1%,[32] Sweden 6.8%[18] (0% Västra Götaland, Halland, Malmö, and Jönköping[33] - 19.5% Västerbotten[34]), Han Chinese 6.77% (0% to 21.4%),[25], Koreans 6.58% (4.41% to 12%) 12% Koreans, [35] 6.58% Koreans from KPGP(Korean Genome Project), [36], 6.9% Jeju[20] 6.4% Gochang [37] 6.3% Gangwon [20] 5.7% North Korean [38] 4.8% Gyeongsang,[20] 4.4% Jeolla,[20] 4.2% Chungcheong,[20] 4.0% Seoul,[39] 3.0% Daejeon,[39] 1.8% Seoul-Gyeonggi,[20] Ulchi 5.8%,[40] Tibetans 5.65%,[41] Kazakhs 5.33% [42] (Suan 0%, Qangly 0%, Oshaqty 0%, Jetyru 1.2%, Dulat 1.6%, Argyn 2.0%, Alimuly 2.5%, Ysty 3.5%, Baiuly 3.9%, Alban 4.3%, Qongyrat 7.4%, Qypshaq 10.3%, Jalair 10.9%, Qozha 16.7%, Syrgeli 65.6%), Northern Thai 5.2%,[43] Uyghurs 4.89% (2.8%,[44] 4.8%,[25] 4.99%,[45] 6.0%,[21] 8.6%[14]), Kyrgyz 3.9% (2.8% Kyzylsu,[46] 3.3% Kyzylsu,[47] 4.5% Kyrgyzstan,[27] 10% Urumqi[46]), Vietnamese 3.4%, Japanese 1.9% (0%,[2] 0.8%,[48] 0.9%,[49] 1.7%,[50] 2.5%,[20] 4.3%,[51] 4.8%,[21] 6.4%[14])

It is most commonly found in males originating from northern Eurasia. It also has been observed at lower frequencies in populations native to other regions, including parts of the Balkans, Central Asia, East Asia, and Southeast Asia.

Origins

 
Estimated prehistoric migration routes for Y-chromosome haplogroup N lineage.[52]

Haplogroup NO-M214 – its most recent common ancestor with its sibling, haplogroup O-M175 – is estimated to have existed about 36,800–44,700 years ago.[1][53][2]

It is generally considered that N-M231 arose in East Asia approximately 19,400 (±4,800) years ago and populated northern Eurasia after the Last Glacial Maximum. Males carrying the marker apparently moved northwards as the climate warmed in the Holocene, migrating in a counter-clockwise path, to eventually become concentrated in areas as far away as Fennoscandia and the Baltic (Rootsi et al. 2006). The apparent dearth of haplogroup N-M231 amongst Native American peoples indicates that it spread after Beringia was submerged (Chiaroni, Underhill & Cavalli-Sforza 2009), about 11,000 years ago.

Distribution

 
Projected distributions of haplogroup N sub-haplogroups.[52] (A) N*-M231, (B) N1*-LLY22g, (C) N1a-M128, (D) N1b-P43, (E) N1c-M46.

Haplogroup N has a wide geographic distribution throughout northern Eurasia, and it also has been observed occasionally in other areas, including Central Asia and the Balkans.

It has been found with greatest frequency among indigenous peoples of Russia, including Finnic peoples, Mari, Udmurt, Komi, Khanty, Mansi, Nenets, Nganasans, Turkic peoples (Yakuts, Dolgans, Khakasses, Tuvans, Tatars, Chuvashes, etc.), Buryats, Tungusic peoples (Evenks, Evens, Negidals, Nanais, etc.), Yukaghirs, Luoravetlans (Chukchis, Koryaks), and Siberian Eskimos, but certain subclades are very common in Finland, Estonia, Latvia, and Lithuania, and other subclades are found at low frequency in China (Yi, Naxi, Lhoba, Han Chinese, etc.).[54] Especially in ethnic Finnic peoples and Baltic-speaking peoples of northern Europe, the Ob-Ugric-speaking and Northern Samoyed peoples of western Siberia, and Turkic-speaking peoples of Russia (especially Yakuts (McDonald 2005), but also Altaians, Shors, Khakas, Chuvashes, Tatars, and Bashkirs). Nearly all members of haplogroup N among these populations of northern Eurasia belong to subclades of either haplogroup N-Tat or haplogroup N-P43.

Y-chromosomes belonging to N1b-F2930/M1881/V3743, or N1*-CTS11499/L735/M2291(xN1a-F1206/M2013/S11466), have been found in China and sporadically throughout other parts of Eurasia. N1a-F1206/M2013/S11466 is found in high numbers in Northern Eurasia.

N2-Y6503, the other primary subclade of haplogroup N, is extremely rare and is mainly represented among extant humans by a recently formed subclade that is virtually restricted to the countries making up the former Yugoslavia (Bosnia-Herzegovina, Croatia, Serbia, and Montenegro), Hungary and Austria. Other members of N2-Y6503 include a Hungarian with recent ancestry from Suceava in Bukovina, a Slovakian, a few British individuals, and an Altaian.[1]

N* (M231)

Y-chromosomes that display the M231 mutation that defines Haplogroup N-M231, but do not display the CTS11499, L735, M2291 mutations that define Haplogroup N1 are said to belong to paragroup N-M231*.[4]

N-M231* has been found at low levels in China.[4] Out of a sample of 165 Han males from China, two individuals (1.2%) were found to belong to N*.(Karafet et al. 2010).[Footnote 1] One originated from Guangzhou and one from Xi'an.[citation needed]

Among the ancient samples from the Baikal Early Neolithic Kitoi culture, one of the Shamanka II samples (DA250), dated to c. 6500 BP, was analyzed as NO1-M214.[55]

N1 (CTS11499, Z4762, CTS3750)

In 2014, there was a major change in the definition of subclade N1, when LLY22g was retired as the main defining SNP for N1 because of reports of LLY22g's unreliability. According to ISOGG, LLY22g is problematic because it is a "palindromic marker and can easily be misinterpreted."[4] Since then, the name N1 has been applied to a clade marked by a great number of SNPs, including CTS11499, Z4762, and CTS3750. N1 is the most recent common ancestor of all extant members of Haplogroup N-M231 except members of the rare N2-Y6503 (N2-B482) subclade. The TMRCA of N1 is estimated to be 18,000 years before present (16,300–19,700 BP; 95% CI).[1] Since the revision of 2014, the position of many examples of "N1-LLY22g" within haplogroup N have become unclear. Therefore, it is better to check yfull and ISOGG 2019 in order to understand the updated structure of N-M231.

However, in older studies, N-LLY22g has been reported to reach a frequency of up to 30% (13/43) among the Yi people of Butuo County, Sichuan in Southwest China (Hammer et al. 2005, Karafet et al. 2001, and Wen et al. 2004). It is also found in 34.6% of Lhoba people (Wen et al. 2004).[56] N1-LLY22g* has been found in samples of Han Chinese, but with widely varying frequency:

Other populations in which representatives of N1*-LLY22g have been found include:

N1(xN1a,N1c) was found in ancient bones of Liao civilization:[57]

N-CTS4309: two people identified with this subgroup in Iraq. Very rare.

N1a (F1206/M2013/S11466)

The N1a2-F1008/L666 clade and N1a1-M46/Page70/Tat are estimated to share a most recent common ancestor in N1a-F1206/M2013/S11466 approximately 15,900 [95% CI 13,900 <-> 17,900] years before present[1] or 17,621 [95% CI 14,952 <-> 20,282] years before present.[3]

N1a1 (M46/Page70/Tat, L395/M2080)

All M46 in Yfull database are M178, being a quarter younger than separation from F1139.[58]

The mutations that define the subclade N-M46[Phylogenetics 2] are M46/Tat and P105. This is the most frequent subclade of N. It probably arose in a Northeast Asian population, because the oldest ancient samples comply with this genetic profile.[59][60] N has experienced serial bottlenecks in Siberia and secondary expansions in eastern Europe (Rootsi et al. 2006). Haplogroup N-M46 is approximately 14,000 years old.

In Siberia, haplogroup N-M46 reaches a maximum frequency of approximately 90% among the Yakuts, a Turkic people who live mainly in the Sakha (Yakutia) Republic. However, N-M46 is present with much lower frequency among many of the Yakuts' neighbors, such as Evenks and Evens.[8] It also has been detected in 5.9% (3/51) of a sample of Hmong Daw from Laos (Cai 2011), 2.4% (2/85) of a sample from Seoul, South Korea (Katoh 2004), and in 1.4% (1/70) of a sample from Tokushima, Japan (Hammer et al. 2005).

The haplogroup N-M46 has a low diversity among Yakuts suggestive of a population bottleneck or founder effect (Pakendorf 2002). This was confirmed by a study of ancient DNA which traced the origins of the male Yakut lineages to a small group of horse-riders from the Cis-Baikal area (Crubézy 2010).

N-Tat has been observed with greatly varying frequency in samples from Sweden. Karlsson et al. (2006) found N-Tat in 44.7% (17/38) of a sample of Saami nomads from Jokkmokk, 19.5% (8/41) of a sample from Västerbotten, 14.5% (8/55) of a sample from Uppsala, 10.0% (4/40) of a sample from Gotland, 9.5% (4/42) of a sample from Värmland, 7.3% (3/41) of a sample from Östergötland/Jönköping, 2.4% (1/41) of a sample from Blekinge/Kristianstad, and 2.2% (1/45) of a sample from Skaraborg.[34]

Lappalainen et al. (2008) found N-Tat in 14.4% (23/160) of a sample from Sweden.[13]

Lappalainen et al. (2009) found N-Tat in 15.4% (4/26) of a sample from Södermanland, 12.5% (3/24) of a sample from Västmanland, 12.1% (4/33) of a sample from Uppsala, 7.8% (4/51) of a sample from Gothenburg, 7.0% (3/43) of a sample from Norrbotten, 6.8% (5/73) of a sample from Skåne, 6.6% (15/228) of a sample from Stockholm, 6.3% (3/48) of a sample from Sydnorrland, 6.3% (2/32) of a sample from Västerbotten, 6.3% (2/32) of a sample from Örebro, 5.9% (3/51) of a sample from Värmland/Dalarna, 5.4% (2/37) of a sample from Östra Götaland, and 5.1% (2/39) of a sample from southeastern Sweden (Kalmar, Gotland, Kronoberg, and Blekinge). They did not find any instance of N-Tat in their samples from Jönköping (0/28), Malmö (0/29), Halland (0/34), or Västra Götaland (0/75).[33]

N1a1a (M178)

The subclade N-M178[Phylogenetics 3] is defined by the presence of markers M178 and P298. N-M178* has higher average frequency in Northern Europe than in Siberia, reaching frequencies of approximately 60% among Finns and approximately 40% among Latvians, Lithuanians & 35% among Estonians (Derenko 2007 and Lappalainen 2008).

Miroslava Derenko and her colleagues noted that there are two subclusters within this haplogroup, both present in Siberia and Northern Europe, with different histories. The one that they labelled N3a1 first expanded in south Siberia and spread into Northern Europe. Meanwhile, the younger subcluster, which they labelled N3a2, originated in south Siberia (probably in the Baikal region) (Derenko 2007).

N-M178 was also found in two Na-Dené speaking Tłı̨chǫs in North America.[61]

Neolithic samples from Baikal area have yielded plenty of yDNA N specimens, and one sample from Fofonovo, Buryatia, 5000-4000 BC is among the first Tat samples in the ancient record.[59]

Earliest samples of N1a1a-L708 were found in Trans-Baikal (brn008, N1a1a1*-L708; brn003, N1a1a1a1*-M2126) between 8,000 and 6,000 YBP. Downstream samples were found in Yakutia (N4b2, N1a1a1a1a*-Z1979) and Krasnoyarsk Krai (kra001, N1a1a1a1a*-L392), between 5,000 and 4,000 YBP.[62][63]

N1a2 (F1008/L666)

N1a2a-M128 and N1a2b-B523/P43 are estimated to share a most recent common ancestor in N1a2-F1008/L666 approximately 8,600 [95% CI 7,500 <-> 9,800] years before present,[1] 9,200 years before present,[64] or 9,314 [95% CI 7,419 <-> 11,264] years before present.[3]

At least three of six tested male specimens from the Early Neolithic (ceramic-using hunter-gatherer of approximately 7200–6200 years ago) layer at the Shamanka archaeological site near the southern end of Lake Baikal have been found to belong to N1a2-L666.[55]

N1a2a-M128

Haplogroup N-M128
 
Possible place of originAsia
AncestorN1a2 (F1008/L666)
DescendantsF710, F1998
Defining mutationsM128
Highest frequenciesManchus 2.5% (Liaoning 3.45%~3.9%, Jilin 0.0%), Koreans 1.1% (Liaoning 2.4%, Jilin 2.0~2.5%, Gyeongsang 1.2%, Jeolla 1.1%, Chungcheong 0.9%, Seoul 0.3%), Xibe 1.0%, Han 0.89% (Shanxi 1.83%, Henan 1.53%, Gansu 1.46%, Hebei 1.41%, Shaanxi 1.40%, Tianjin 1.38%, Shandong 1.17%, Beijing 1.14%, Inner Mongolia 1.13%, Heilungjiang 1.12%, Liaoning 1.12%, Fujian 1.12%, Anhui 0.93%, Jilin 0.86%, Ningxia 0.82%, Jiangsu 0.81%, Yunnan 0.79%, Hubei 0.77%, Zhejiang 0.73%, Taiwan 0.70%, Sichuan 0.54%, Hunan 0.52%, Chungqing 0.51%, Guizhou 0.51%, Guangdong 0.45%, Hainan 0.43%, Xinjiang 0.43%, Shanghai 0.36%, Jiangxi 0.34%, Guangxi 0.23%, Qinghai 0.18%), Mongolians 0.7% (Liaoning 1.9%, Horqin 0.3%, Ulaanbaatar 0.0%), Japanese 0.3% (Tokushima 3.5%, Ibaraki 2.0%, Hiroshima 1.3%, Nagoya 1.0%, Osaka 0.2%, Tokyo 0.0%, Shizuoka 0.0%, Yamaguchi 0.0%), Kazakhs 0.1% (Khoja 1.9%, Baiuly 0.6%, Uysun 0.4%)

This subclade is defined by the presence of the marker M128.[Phylogenetics 4] N-M128 was first identified in a sample from Japan (1/23 = 4.3%) and in a sample from Central Asia and Siberia (1/184 = 0.5%) in a preliminary survey of worldwide Y-DNA variation.[51] Subsequently, it has been found with low frequency in some samples of the Manchu people, Sibe people, Evenks, Koreans, Han Chinese, Hui, Tibetans, Vietnamese, Bouyei people, Kazakhs, Uzbeks, Uyghurs, Salars, Tu, Mongols, the Buzava tribe of Kalmyks,[29] Khakas, and Komis.[16]

A number of a Han Chinese, an Ooled Mongol, a Qiang, and a Tibetan were found to belong to a sister branch (or branches) of N-M128 under paragroup N-F1154*.[65]

A neolithic sample brn002 (~5,940 BP) in Trans-Baikal was discovered to be an early offshoot upstream of N-M128.[66][62]

As a genetic testing result of Yelü clan, a royal family of the Liao Dynasty and Khitan descents, it was found to belong to N-F1998, a downstream of N-M128.

N1a2b (P43)

Haplogroup N-P43[Phylogenetics 5] is defined by the presence of the marker P43. It has been estimated to be approximately 4,000 to 5,500 years old (TMRCA 4,510 years,[64] TMRCA 4,700 [95% CI 3,800 <-> 5,600] ybp,[1] or 4,727 [95% CI 3,824 <-> 5,693] years before present[3]). It has been found very frequently among Northern Samoyedic peoples, speakers of Ob-Ugric languages, and northern Khakassians, and it also has been observed with low to moderate frequency among speakers of some other Uralic languages, Turkic peoples, Mongolic peoples, Tungusic peoples, and Siberian Yupik people.

The highest frequencies of N-P43 are observed among north-west Siberian populations: 92% (35/38)[16] in a sample of Nganasan, 78% (7/9)[67][18] in a sample of Enets, 78% (21/27)[31] in a sample of Khants, 75% (44/59)[16] in a sample of Tundra Nenets, 69% (29/42)[3] in another sample of Nenets, 60% (15/25)[12] in a sample of Mansi, 57% (64/112)[11] in another sample of Khants, 54% (27/50)[3] in another sample of Nganasan, 45% (40/89)[16] in a sample of Forest Nenets, 38% (18/47)[68] in a third sample of Khants, and 25% (7/28)[12] in a fourth sample of Khants. In Europe, the N-P43 types have their highest frequency of 20% among Volga-Uralic populations. The extreme western border of the spread of N-P43 is Finland, where this haplogroup occurs only at marginal frequency – 0.4%. Yet N-P43 is quite frequent among Vepsas (17.9%), a small Finnic population living in immediate proximity to Finns, Karelians and Estonians.[16]

Haplogroup N-P43 also has been observed with very high frequency (26/29 = 89.7% of a sample from the settlement of Topanov and 19/22 = 86.4% of a sample from the settlement of Malyi Spirin) in samples of Kachins, a Turkic-speaking ethnic group or territorial subgroup of the Khakas people, from Shirinsky District of northern Khakassia.[9] There appears to be a cline through the Sagai (another Turkic-speaking ethnic group that is now considered to be a constituent of the Khakas people), with 46.2% (55/119) of Sagai sampled from Ust'–Es', Esino, Ust'–Chul', and Kyzlas settlements of Askizsky District of central Khakassia belonging to haplogroup N-P43 vs. only 13.6% (11/81) of Sagai sampled from Matur, Anchul', Bol'shaya Seya, and Butrakhty settlements of Tashtypsky District of southern Khakassia belonging to this haplogroup.[9] However, other researchers' samples of Khakas people have exhibited only moderate frequencies of N-P43 or potential N-P43. Derenko et al. (2006) examined a sample of Khakassians (n=53) collected in the settlements of Askiz, Shirinsk, Beisk and Ordzhonikidzevsk districts of Khakass Republic and found that 15 of them (28.3%) belonged to N-LLY22g(xTat).[19] Rootsi et al. (2007) examined a sample of Khakas (n=181) and found that 31 of them (17.1%) belonged to N-P43;[16] (Ilumäe et al. 2016) retested 174 of the individuals in this sample and found that 27 of them (15.5%) belonged to the N-B478 (Asian/northern Samoyedic) subclade of N-P43 and 2 of them (1.1%) belonged to the N-L1419 (European/Volga Finnic and Chuvash) subclade of N-P43 for a total of 29 (16.7%) N-P43.[3]

Haplogroup N-P43 forms two distinctive subclusters of STR haplotypes, Asian and European, the latter mostly distributed among Finno-Ugric-speaking peoples and related populations (Rootsi et al. 2006).

N1a2b1-B478

The TMRCA of N-B478 has been estimated to be 3,007 [95% CI 2,171 <-> 3,970] years before present.[3] It is one of the most prevalent Y-DNA haplogroups among indigenous populations of northwestern Siberia: 69.0% (29/42) Nenets, 50.0% (25/50) Nganasan, 22.2% (12/54) Dolgan from Taymyr, 7.0% (3/43) Selkup, 1.6% (1/63) Ob-Ugrian. It is also quite prevalent among populations of Central Siberia, Southern Siberia, and Mongolia: 17.9% (17/95) Tuvan, 15.5% (27/174) Khakas, 13.0% (6/46) Tozhu Tuvans,[28] 8.7% (2/23) Shor, 8.3% (2/24) Even, 8.2% (5/61) Altaian, 5.3% (3/57) Evenk, 5.0% (19/381) Mongol, 4.9% (3/61) Sart-Kalmak (partial descendants of Oirat Mongols in Kyrgyzstan),[28] 4.2% (9/216) Yakut, 2.1% (1/47) Torgut (Mongolia),[28] 1.4% (1/69) Derbet (Kalmykia),[28] 0.9% (1/111) Buryat. A geographically outlying member has been found in a sample of Chuvash (1/114 = 0.88%).[3]

Karafet et al. (2018) observed N-P63, which appears to be roughly phylogenetically equivalent to N-B478, in 91.2% (31/34) Nganasan, 63.8% (30/47) Tundra Nenets, 42.7% (35/82) Forest Nenets, 14.0% (8/57) Dolgan, 7.0% (9/129) Selkup, 3.3% (3/91) Evenk, 2.7% (2/75) Mongol, 2.6% (2/78) Komi, 2.5% (2/80) Buryat, and 2.0% (2/98) Altai Kizhi.[6] This haplogroup was not observed in samples of Yukaghir (0/10), Koryak (0/11), Teleut (0/40), Ket (0/44), Yakut (0/62), or Khanty (0/165) populations.[6]

N1b (F2930)

Haplogroup N1b has been predominantly found in the Yi people, a Tibeto-Burman speaking ethnic group in southwestern China who originated from ancient Qiang tribes in northwestern China.[54] However, it also has been found in people all over China and in some samples of people from Poland, Belarus, Russia, Mongolia, Korea, Japan, Vietnam, Cambodia, Bhutan, and India.

N2 (Y6503)

N2 (Y6503/FGC28528; B482/FGC28394/Y6584) – a primary branch of haplogroup N-M231, is now represented mainly by a subclade, N-FGC28435, that has spread probably some time in the first half of the second millennium CE[69] and that has been found in individuals from Serbia, Croatia, Bosnia and Herzegovina, Montenegro, and Turkey (Istanbul).[70][69]

N-Y7310 (or N-F14667) subsumes N-FGC28435 and likewise probably descends from a common ancestor who has lived some time in the first half of the last millennium. However, members of N-Y7310(xFGC28435) exhibit a greater geographic range, including an individual from Rostov Oblast of Russia and a Romanian Hungarian individual with ancestry from Suceava, Bukovina.[1]

Other branches of N-P189 include members from Turkey,[1] Russia (Moscow Oblast[1]), France (Charente-Maritime[1]), and England (Devon[1]).[71] The most recent common ancestor of all the aforementioned extant N-P189 lineages has been estimated to be 4,900 (95% CI 5,700 <-> 4,100) years before present.[1] An archaeological specimen attributed to the Botai culture of northern Kazakhstan and dated to the latter half of the fourth millennium BCE belongs to N-P189*, being basal to present-day European members of N-P189.[72][1]

Lineages that belong to N-Y6503(xP189) and are only distantly related (with a time to most recent common ancestor estimated to be greater than 10,000 years before present[1]) to the aforementioned members of N-P189 have been found in an individual from the present-day Altai Republic[1] and probably also in an archaeological specimen attributed to the Iron Age Mezőcsát culture of what is now Hungary (approx. 2,900 years before present)[73] and in an archaeological specimen attributed to the Kitoi culture of ceramic-using foragers of the area around Lake Baikal (approx. 6,700 years before present).[72]

Ancient peoples

A sample excavated at the Houtaomuga site in the Yonghe neighborhood of Honggangzi Township, Da'an, Jilin, China dating back to 7430–7320 years ago (Phase II of the Early Neolithic) has been found to belong to Y-DNA haplogroup N and mtDNA haplogroup B4c1a2. This sample is autosomally identical with the Neolithic Amur River Basin populations, of which Nivkh people are the closest modern representative. As the paper detected this ancestry in terminal Pleistocene USR1 specimen in Alaska, it is therefore, postulated that there was gene flow from Amur to America of a population belonging to a hypothetical Chukotko-Kamchatkan–Nivkh linguistic family.[60]

N has also been found in many samples of Neolithic human remains exhumed from Liao civilization in northeastern China, and in the circum-Baikal area of southern Siberia.[74] It is suggested that yDNA N, reached southern Siberia from 12-14 kya. From there it reached southern Europe 8-10kya.[52]

Phylogeny

Phylogenetic tree

In the following tree the nomenclature of three sources is separated by slashes: ISOGG Tree 10 December 2017 (ver.12.317)

History of phylogenetic nomenclature

Prior to 2002, there were in academic literature at least seven naming systems for the Y-Chromosome Phylogenetic tree. This led to considerable confusion. In 2002, the major research groups came together and formed the Y-Chromosome Consortium (YCC). They published a joint paper that created a single new tree that all agreed to use. Later, a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely. The table below brings together all of these works at the point of the landmark 2002 YCC Tree. This allows a researcher reviewing older published literature to quickly move between nomenclatures.

YCC 2002/2008 (Shorthand) (α) (β) (γ) (δ) (ε) (ζ) (η) YCC 2002 (Longhand) YCC 2005 (Longhand) YCC 2008 (Longhand) YCC 2010r (Longhand) ISOGG 2006 ISOGG 2007 ISOGG 2008 ISOGG 2009 ISOGG 2010 ISOGG 2011 ISOGG 2012
N-LLY22g 12 VIII 1U 25 Eu16 H5 F N* N N1 N1 - - - - - - -
N-M128 12 VIII 1U 25 Eu16 H5 F N1 N1 N1a N1a - - - - - - -
N-P63 12 VIII 1U 25 Eu16 H5 F N2 N2a N1b1 N1b1 - - - - - - -
N-TAT 12 VIII 1I 26 Eu13 H5 F N3* N3 N1c N1c - - - - - - -
N-M178 16 VIII 1I 26 Eu14 H5 F N3a* M178 N1c1 N1c1 - - - - - - -
N-P21 16 VIII 1I 26 Eu14 H5 F N3a1 N3a1 N1c1a N1c1a - - - - - - -

Sources The following research teams per their publications were represented in the creation of the YCC Tree.

Unreliable mutations (SNPs and UEPs)

The b2/b3 deletion in the AZFc region of the Y-chromosome appears to have occurred independently on at least four different occasions. Therefore, this deletion should not be taken as a unique event polymorphism defining this branch of the Y-chromosome tree (ISOGG 2012).

Links to genetics concepts

Y-DNA N subclades

  • N-M231

Y-DNA backbone tree

Footnotes

References

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  • Derenko M, Malyarchuk B, Denisova G, Wozniak M, Grzybowski T, Dambueva I, Zakharov I (2007). "Y-chromosome haplogroup N dispersals from south Siberia to Europe". Journal of Human Genetics. 52 (9): 763–770. doi:10.1007/s10038-007-0179-5. PMID 17703276.
  • Gayden T, Cadenas AM, Regueiro M, Singh NB, Zhivotovsky LA, Underhill PA, et al. (May 2007). "The Himalayas as a directional barrier to gene flow". American Journal of Human Genetics. 80 (5): 884–894. doi:10.1086/516757. PMC 1852741. PMID 17436243.
  • Hammer MF, Karafet TM, Park H, Omoto K, Harihara S, Stoneking M, Horai S (2005). "Dual origins of the Japanese: common ground for hunter-gatherer and farmer Y chromosomes". Journal of Human Genetics. 51 (1): 47–58. doi:10.1007/s10038-005-0322-0. PMID 16328082.
  • Ilumäe AM, Reidla M, Chukhryaeva M, Järve M, Post H, Karmin M, et al. (July 2016). "Human Y Chromosome Haplogroup N: A Non-trivial Time-Resolved Phylogeography that Cuts across Language Families". American Journal of Human Genetics. 99 (1): 163–173. doi:10.1016/j.ajhg.2016.05.025. PMC 5005449. PMID 27392075.
  • Kang Hu; Shi Yan; Kai Liu; Chao Ning; Lan-Hai Wei; Shi-Lin Li; Bing Song; Ge Yu; Feng Chen; Li-Jun Liu; Zhi-Peng Zhao; Chuan-Chao Wang; Ya-Jun Yang; Zhen-Dong Qin; Jing-Ze Tan; Fu-Zhong Xue; Hui Li; Long-Li Kang; Li Jin (2015). "The dichotomy structure of Haplogroup N". arXiv:1504.06463 [q-bio.PE].
  • Karafet T, Xu L, Du R, Wang W, Feng S, Wells RS, et al. (September 2001). "Paternal population history of East Asia: sources, patterns, and microevolutionary processes". American Journal of Human Genetics. 69 (3): 615–628. doi:10.1086/323299. PMC 1235490. PMID 11481588. In this article, the "Southern Han" sample of Karafet and Hammer's research group is described as originating from Guangdong, and the "Northern Han" sample is described as originating from Shaanxi.
  • Karafet TM, Mendez FL, Meilerman MB, Underhill PA, Zegura SL, Hammer MF (May 2008). "New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree". Genome Research. 18 (5): 830–838. doi:10.1101/gr.7172008. PMC 2336805. PMID 18385274.
  • Karafet TM, Hallmark B, Cox MP, Sudoyo H, Downey S, Lansing JS, Hammer MF (August 2010). "Major east-west division underlies Y chromosome stratification across Indonesia". Molecular Biology and Evolution. 27 (8): 1833–1844. doi:10.1093/molbev/msq063. PMID 20207712.
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  • Lappalainen T, Laitinen V, Salmela E, Andersen P, Huoponen K, Savontaus ML, Lahermo P (May 2008). "Migration waves to the Baltic Sea region". Annals of Human Genetics. 72 (Pt 3): 337–348. doi:10.1111/j.1469-1809.2007.00429.x. PMID 18294359. S2CID 32079904.
  • Malyarchuk B, Derenko M, Grzybowski T, Lunkina A, Czarny J, Rychkov S, et al. (December 2004). "Differentiation of mitochondrial DNA and Y chromosomes in Russian populations". Human Biology. 76 (6): 877–900. doi:10.1353/hub.2005.0021. PMID 15974299. S2CID 17385503.
  • Pakendorf B, Morar B, Tarskaia LA, Kayser M, Soodyall H, Rodewald A, Stoneking M (February 2002). "Y-chromosomal evidence for a strong reduction in male population size of Yakuts". Human Genetics. 110 (2): 198–200. doi:10.1007/s00439-001-0664-4. PMID 11935328. S2CID 30671159.
  • Rootsi S, Zhivotovsky LA, Baldovič M, Kayser M, Kutuev IA, Khusainova R, et al. (6 December 2006). "A counter-clockwise northern route of the Y-chromosome haplogroup N from Southeast Asia towards Europe". European Journal of Human Genetics. 15 (2): 204–211. doi:10.1038/sj.ejhg.5201748. PMID 17149388.
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Websites

  • ISOGG (2012). "Y-DNA Haplogroup Tree 2012".
  • McDonald D (2004). (PDF). Archived from the original (PDF) on 2004-07-28. Retrieved 2009-08-29.

Sources for conversion tables

  • Capelli, Cristian; Wilson, James F.; Richards, Martin; Stumpf, Michael P.H.; et al. (February 2001). "A Predominantly Indigenous Paternal Heritage for the Austronesian-Speaking Peoples of Insular Southeast Asia and Oceania". The American Journal of Human Genetics. 68 (2): 432–443. doi:10.1086/318205. PMID 11170891.
  • Hammer, Michael F.; Karafet, Tatiana M.; Redd, Alan J.; Jarjanazi, Hamdi; et al. (1 July 2001). "Hierarchical Patterns of Global Human Y-Chromosome Diversity". Molecular Biology and Evolution. 18 (7): 1189–1203. doi:10.1093/oxfordjournals.molbev.a003906. PMID 11420360.
  • Jobling, Mark A.; Tyler-Smith, Chris (2000), "New uses for new haplotypes", Trends in Genetics, 16 (8): 356–62, doi:10.1016/S0168-9525(00)02057-6, PMID 10904265
  • Kaladjieva, Luba; Calafell, Francesc; Jobling, Mark A; Angelicheva, Dora; et al. (February 2001). "Patterns of inter- and intra-group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineages". European Journal of Human Genetics. 9 (2): 97–104. doi:10.1038/sj.ejhg.5200597. PMID 11313742.
  • Semino O, Passarino G, Oefner PJ, Lin AA, et al. (2000), "The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans: A Y Chromosome Perspective", Science, 290 (5494): 1155–1159, Bibcode:2000Sci...290.1155S, doi:10.1126/science.290.5494.1155, PMID 11073453
  • Su, Bing; Xiao, Junhua; Underhill, Peter; Deka, Ranjan; et al. (December 1999). "Y-Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age". The American Journal of Human Genetics. 65 (6): 1718–1724. doi:10.1086/302680. PMC 1288383. PMID 10577926.
  • Underhill PA, Shen P, Lin AA, Jin L, et al. (November 2000). "Y chromosome sequence variation and the history of human populations". Nature Genetics. 26 (3): 358–361. doi:10.1038/81685. PMID 11062480. S2CID 12893406.

Further reading

Phylogenetics

  1. ^ The b2/b3 deletion in the AZFc region of the human Y-chromosome is a characteristic of Haplogroup N-M231 haplotypes. This deletion, however, appears to have occurred independently on four different occasions. Therefore this deletion should not be thought as a unique event polymorphism contributing to the definition of this branch of the Y-chromosome tree (ISOGG 2012).
  2. ^ This table shows historic names for N-M46 (AKA N-Tat) from peer reviewed literature.
    YCC 2002/2008 (Shorthand) N-M46/N-TAT
    Jobling and Tyler-Smith 2000 12
    Underhill 2000 VIII
    Hammer 2001 1I
    Karafet 2001 26
    Semino 2000 Eu13
    Su 1999 H5
    Capelli 2001 F
    YCC 2002 (Longhand) N3*
    YCC 2005 (Longhand) N3
    YCC 2008 (Longhand) N1c
    YCC 2010r (Longhand) N1c
  3. ^ This table shows historic names for N-M178 from peer reviewed literature.
    YCC 2002/2008 (Shorthand) N-M178
    Jobling and Tyler-Smith 2000 16
    Underhill 2000 VIII
    Hammer 2001 1I
    Karafet 2001 26
    Semino 2000 Eu14
    Su 1999 H5
    Capelli 2001 F
    YCC 2002 (Longhand) N3a*
    YCC 2005 (Longhand) M178
    YCC 2008 (Longhand) N1c1
    YCC 2010r (Longhand) N1c1
  4. ^ This table shows historic names for N-M128 from peer reviewed literature.
    YCC 2002/2008 (Shorthand) N-M128
    Jobling and Tyler-Smith 2000 12
    Underhill 2000 VIII
    Hammer 2001 1U
    Karafet 2001 25
    Semino 2000 Eu16
    Su 1999 H5
    Capelli 2001 F
    YCC 2002 (Longhand) N1
    YCC 2005 (Longhand) N1
    YCC 2008 (Longhand) N1a
    YCC 2010r (Longhand) N1a
  5. ^ This branch is sometimes called N1b in early trees.

External links

  • , from The Genographic Project, National Geographic
  • N North Eurasian YDNA Project at FamilyTreeDNA
  • N Y-DNA Haplogroup Project at FamilyTreeDNA
  • N1c1 Y-DNA Haplogroup Project at FamilyTreeDNA
  • Rurikid Dynasty DNA Project at FamilyTreeDNA
  • Russian Nobility DNA Project at FamilyTreeDNA

haplogroup, m231, this, article, about, human, haplogroup, human, mtdna, haplogroup, haplogroup, mtdna, this, article, possibly, contains, original, research, please, improve, verifying, claims, made, adding, inline, citations, statements, consisting, only, or. This article is about the human Y DNA haplogroup For the human mtDNA haplogroup see Haplogroup N mtDNA This article possibly contains original research Please improve it by verifying the claims made and adding inline citations Statements consisting only of original research should be removed November 2021 Learn how and when to remove this template message Haplogroup N M231 is a Y chromosome DNA haplogroup defined by the presence of the single nucleotide polymorphism SNP marker M231 Phylogenetics 1 Haplogroup NPossible time of origin36 800 95 CI 34 300 39 300 years before present YFull 1 44 700 or 38 300 ybp depending on mutation rate 2 41 900 95 CI 40 175 43 591 ybp 3 Coalescence age21 700 95 CI 19 500 23 900 ybp YFull 1 25 313 95 CI 21 722 28 956 ybp 3 Possible place of originNorthern East Asia 4 5 AncestorNODefining mutationsM231Highest frequenciesNganassan 58 3 94 1 6 Yakuts 81 8 7 94 6 8 Xu 2015 harv error no target CITEREFXu2015 help Khakass Shirinsky District 90 2 9 Siberian Tatars Zabolotnie Tatars 89 5 10 Ugrians 77 8 3 Khanty 64 3 11 89 3 12 Mansi 76 12 Udmurts 77 8 3 Khakas 41 3 65 11 Komi 33 3 11 79 5 6 Nenets 75 92 9 3 Tundra Nenets 97 9 6 Forest Nenets 98 8 6 Vepsians 55 3 Finns 42 6 West 13 70 9 East 13 or approx 54 3 Tuvans 27 2 54 5 Kharkov 2013 harv error no target CITEREFKharkov2013 help Nanai 46 2 14 15 3 20 Hezhe in the PRC 14 44 6 Nanai in Russia 3 83 8 members of the Samar clan in the Gorin area of the Khabarovsk Territory 15 Karelians 37 1 16 53 8 13 Arkhangelsk Russians 42 6 Arkhangelsk 44 3 3 Pinega 40 8 3 Lithuanian 40 5 3 44 5 13 Latvian approx 42 41 6 13 42 1 17 43 0 3 Mari 41 2 3 Saami 40 Chuvash 33 7 18 36 3 Buryats 34 5 20 2 19 25 0 20 30 9 21 48 0 22 Koryaks 33 3 6 Estonian 30 6 3 33 9 13 Volga Tatars 27 8 3 Teleuts 25 0 6 Northern Altaians 21 8 18 0 11 23 24 6 24 Pskov Russians 22 7 3 Bashkirs 17 3 3 Sibe 17 1 14 18 0 25 Mordvins 12 5 10 3 13 3 3 Mongols 11 26 21 14 20 27 28 Kalmyks 10 4 Torguud 3 4 Derbet 5 1 Buzava 5 3 Khoshut 38 2 29 28 Manchus 10 5 8 21 8 1 30 9 1 25 11 6 25 12 5 25 14 3 14 Belarusians 9 7 3 Central Southern Russians 9 1 Tver 13 2 31 Kursk 12 5 31 13 3 3 Belgorod 11 9 3 Kostroma 11 8 3 Smolensk 7 0 3 Voronezh 6 3 3 Oryol 5 5 3 Ukrainians 9 0 3 Southern Altaians 7 1 4 2 24 9 7 11 Mulam 7 1 32 Sweden 6 8 18 0 Vastra Gotaland Halland Malmo and Jonkoping 33 19 5 Vasterbotten 34 Han Chinese 6 77 0 to 21 4 25 Koreans 6 58 4 41 to 12 12 Koreans 35 6 58 Koreans from KPGP Korean Genome Project 36 6 9 Jeju 20 6 4 Gochang 37 6 3 Gangwon 20 5 7 North Korean 38 4 8 Gyeongsang 20 4 4 Jeolla 20 4 2 Chungcheong 20 4 0 Seoul 39 3 0 Daejeon 39 1 8 Seoul Gyeonggi 20 Ulchi 5 8 40 Tibetans 5 65 41 Kazakhs 5 33 42 Suan 0 Qangly 0 Oshaqty 0 Jetyru 1 2 Dulat 1 6 Argyn 2 0 Alimuly 2 5 Ysty 3 5 Baiuly 3 9 Alban 4 3 Qongyrat 7 4 Qypshaq 10 3 Jalair 10 9 Qozha 16 7 Syrgeli 65 6 Northern Thai 5 2 43 Uyghurs 4 89 2 8 44 4 8 25 4 99 45 6 0 21 8 6 14 Kyrgyz 3 9 2 8 Kyzylsu 46 3 3 Kyzylsu 47 4 5 Kyrgyzstan 27 10 Urumqi 46 Vietnamese 3 4 Japanese 1 9 0 2 0 8 48 0 9 49 1 7 50 2 5 20 4 3 51 4 8 21 6 4 14 It is most commonly found in males originating from northern Eurasia It also has been observed at lower frequencies in populations native to other regions including parts of the Balkans Central Asia East Asia and Southeast Asia Contents 1 Origins 2 Distribution 2 1 N M231 2 2 N1 CTS11499 Z4762 CTS3750 2 3 N1a F1206 M2013 S11466 2 4 N1a1 M46 Page70 Tat L395 M2080 2 5 N1a1a M178 2 6 N1a2 F1008 L666 2 7 N1a2a M128 2 8 N1a2b P43 2 9 N1a2b1 B478 2 10 N1b F2930 2 11 N2 Y6503 2 12 Ancient peoples 3 Phylogeny 3 1 Phylogenetic tree 3 2 History of phylogenetic nomenclature 3 3 Links to genetics concepts 3 4 Y DNA N subclades 3 5 Y DNA backbone tree 4 Footnotes 5 References 6 Bibliography 6 1 Sources for conversion tables 6 2 Further reading 6 3 Phylogenetics 7 External linksOrigins Edit Estimated prehistoric migration routes for Y chromosome haplogroup N lineage 52 Haplogroup NO M214 its most recent common ancestor with its sibling haplogroup O M175 is estimated to have existed about 36 800 44 700 years ago 1 53 2 It is generally considered that N M231 arose in East Asia approximately 19 400 4 800 years ago and populated northern Eurasia after the Last Glacial Maximum Males carrying the marker apparently moved northwards as the climate warmed in the Holocene migrating in a counter clockwise path to eventually become concentrated in areas as far away as Fennoscandia and the Baltic Rootsi et al 2006 The apparent dearth of haplogroup N M231 amongst Native American peoples indicates that it spread after Beringia was submerged Chiaroni Underhill amp Cavalli Sforza 2009 about 11 000 years ago Distribution Edit Projected distributions of haplogroup N sub haplogroups 52 A N M231 B N1 LLY22g C N1a M128 D N1b P43 E N1c M46 Haplogroup N has a wide geographic distribution throughout northern Eurasia and it also has been observed occasionally in other areas including Central Asia and the Balkans It has been found with greatest frequency among indigenous peoples of Russia including Finnic peoples Mari Udmurt Komi Khanty Mansi Nenets Nganasans Turkic peoples Yakuts Dolgans Khakasses Tuvans Tatars Chuvashes etc Buryats Tungusic peoples Evenks Evens Negidals Nanais etc Yukaghirs Luoravetlans Chukchis Koryaks and Siberian Eskimos but certain subclades are very common in Finland Estonia Latvia and Lithuania and other subclades are found at low frequency in China Yi Naxi Lhoba Han Chinese etc 54 Especially in ethnic Finnic peoples and Baltic speaking peoples of northern Europe the Ob Ugric speaking and Northern Samoyed peoples of western Siberia and Turkic speaking peoples of Russia especially Yakuts McDonald 2005 harv error no target CITEREFMcDonald2005 help but also Altaians Shors Khakas Chuvashes Tatars and Bashkirs Nearly all members of haplogroup N among these populations of northern Eurasia belong to subclades of either haplogroup N Tat or haplogroup N P43 Y chromosomes belonging to N1b F2930 M1881 V3743 or N1 CTS11499 L735 M2291 xN1a F1206 M2013 S11466 have been found in China and sporadically throughout other parts of Eurasia N1a F1206 M2013 S11466 is found in high numbers in Northern Eurasia N2 Y6503 the other primary subclade of haplogroup N is extremely rare and is mainly represented among extant humans by a recently formed subclade that is virtually restricted to the countries making up the former Yugoslavia Bosnia Herzegovina Croatia Serbia and Montenegro Hungary and Austria Other members of N2 Y6503 include a Hungarian with recent ancestry from Suceava in Bukovina a Slovakian a few British individuals and an Altaian 1 N M231 Edit Y chromosomes that display the M231 mutation that defines Haplogroup N M231 but do not display the CTS11499 L735 M2291 mutations that define Haplogroup N1 are said to belong to paragroup N M231 4 N M231 has been found at low levels in China 4 Out of a sample of 165 Han males from China two individuals 1 2 were found to belong to N Karafet et al 2010 Footnote 1 One originated from Guangzhou and one from Xi an citation needed Among the ancient samples from the Baikal Early Neolithic Kitoi culture one of the Shamanka II samples DA250 dated to c 6500 BP was analyzed as NO1 M214 55 N1 CTS11499 Z4762 CTS3750 Edit In 2014 there was a major change in the definition of subclade N1 when LLY22g was retired as the main defining SNP for N1 because of reports of LLY22g s unreliability According to ISOGG LLY22g is problematic because it is a palindromic marker and can easily be misinterpreted 4 Since then the name N1 has been applied to a clade marked by a great number of SNPs including CTS11499 Z4762 and CTS3750 N1 is the most recent common ancestor of all extant members of Haplogroup N M231 except members of the rare N2 Y6503 N2 B482 subclade The TMRCA of N1 is estimated to be 18 000 years before present 16 300 19 700 BP 95 CI 1 Since the revision of 2014 the position of many examples of N1 LLY22g within haplogroup N have become unclear Therefore it is better to check yfull and ISOGG 2019 in order to understand the updated structure of N M231 However in older studies N LLY22g has been reported to reach a frequency of up to 30 13 43 among the Yi people of Butuo County Sichuan in Southwest China Hammer et al 2005 Karafet et al 2001 and Wen et al 2004 It is also found in 34 6 of Lhoba people Wen et al 2004 56 N1 LLY22g has been found in samples of Han Chinese but with widely varying frequency 15 0 6 40 Han from Guangzhou Hammer et al 2005 and Karafet et al 2001 6 8 3 44 Han from Xi an Hammer et al 2005 and Karafet et al 2001 6 7 2 30 Han from Lanzhou Xue et al 2006 3 6 3 84 Taiwanese Han Hammer et al 2005 2 9 1 34 Han from Chengdu Xue et al 2006 2 9 1 35 Han from Harbin Xue et al 2006 2 9 1 35 Han from Meixian District Xue et al 2006 0 0 32 Han from Yining City Xue et al 2006 Other populations in which representatives of N1 LLY22g have been found include Hani people 4 34 11 8 Xue et al 2006 Sibe people 4 41 9 8 Xue et al 2006 Tujia people 2 49 4 1 Hammer et al 2005 Manchu people 2 52 3 8 Hammer et al 2005 to 2 35 5 7 Xue et al 2006 Bit people 1 28 3 6 Cai 2011 harv error no target CITEREFCai2011 help Uyghurs 2 70 2 9 Xue et al 2006 to 2 67 3 0 Hammer et al 2005 Tibetan people 3 105 2 9 Hammer et al 2005 to 3 35 8 6 Xue et al 2006 Koreans 0 106 0 0 2 25 8 Rootsi et al 2006 Xue et al 2006 and Kim 2007harvnb error no target CITEREFKim2007 help Vietnamese people 2 70 2 9 Hammer et al 2005 Japanese people 0 70 Tokushima 2 26 7 7 Aomori Hammer et al 2005 Manchurian Evenks 0 26 0 0 Xue et al 2006 to 1 41 2 4 Hammer et al 2005 Altai people 0 50 Northern to 5 96 5 2 Southern or 0 43 Beshpeltir to 5 46 10 9 Kulada Hammer et al 2005 Kharkov 2007 harv error no target CITEREFKharkov2007 help Shors 2 23 8 7 Rootsi et al 2006 Khakas people 5 181 2 8 Rootsi et al 2006 Tuvans 5 311 1 6 Rootsi et al 2006 Southern Borneo 1 40 2 5 Rootsi et al 2006 Forest Nenets 1 89 1 1 Rootsi et al 2006 Yakuts 0 215 1 121 0 8 Rootsi et al 2006 Turkish people 1 523 0 2 Rootsi et al 2006 In Turkey the total of subclades of haplogroup N M231 amounts to 4 of the male population One individual who belongs either to N or N1 has been found in a sample of 77 males from Kathmandu Nepal 1 77 1 3 N M231 xM128 P43 Tat Gayden 2007 harv error no target CITEREFGayden2007 help N1 xN1a N1c was found in ancient bones of Liao civilization 57 Niuheliang Hongshan Culture 6500 5000 BP 66 7 4 6 Halahaigou Xiaoheyan Culture 5000 4200 BP 100 0 12 12 Dadianzi Lower Xiajiadian culture 4200 3600 BP 60 0 3 5 N CTS4309 two people identified with this subgroup in Iraq Very rare N1a F1206 M2013 S11466 Edit The N1a2 F1008 L666 clade and N1a1 M46 Page70 Tat are estimated to share a most recent common ancestor in N1a F1206 M2013 S11466 approximately 15 900 95 CI 13 900 lt gt 17 900 years before present 1 or 17 621 95 CI 14 952 lt gt 20 282 years before present 3 N1a1 M46 Page70 Tat L395 M2080 Edit All M46 in Yfull database are M178 being a quarter younger than separation from F1139 58 The mutations that define the subclade N M46 Phylogenetics 2 are M46 Tat and P105 This is the most frequent subclade of N It probably arose in a Northeast Asian population because the oldest ancient samples comply with this genetic profile 59 60 N has experienced serial bottlenecks in Siberia and secondary expansions in eastern Europe Rootsi et al 2006 Haplogroup N M46 is approximately 14 000 years old In Siberia haplogroup N M46 reaches a maximum frequency of approximately 90 among the Yakuts a Turkic people who live mainly in the Sakha Yakutia Republic However N M46 is present with much lower frequency among many of the Yakuts neighbors such as Evenks and Evens 8 It also has been detected in 5 9 3 51 of a sample of Hmong Daw from Laos Cai 2011 harv error no target CITEREFCai2011 help 2 4 2 85 of a sample from Seoul South Korea Katoh 2004 harv error no target CITEREFKatoh2004 help and in 1 4 1 70 of a sample from Tokushima Japan Hammer et al 2005 The haplogroup N M46 has a low diversity among Yakuts suggestive of a population bottleneck or founder effect Pakendorf 2002 harv error no target CITEREFPakendorf2002 help This was confirmed by a study of ancient DNA which traced the origins of the male Yakut lineages to a small group of horse riders from the Cis Baikal area Crubezy 2010 harv error no target CITEREFCrubezy2010 help N Tat has been observed with greatly varying frequency in samples from Sweden Karlsson et al 2006 found N Tat in 44 7 17 38 of a sample of Saami nomads from Jokkmokk 19 5 8 41 of a sample from Vasterbotten 14 5 8 55 of a sample from Uppsala 10 0 4 40 of a sample from Gotland 9 5 4 42 of a sample from Varmland 7 3 3 41 of a sample from Ostergotland Jonkoping 2 4 1 41 of a sample from Blekinge Kristianstad and 2 2 1 45 of a sample from Skaraborg 34 Lappalainen et al 2008 found N Tat in 14 4 23 160 of a sample from Sweden 13 Lappalainen et al 2009 found N Tat in 15 4 4 26 of a sample from Sodermanland 12 5 3 24 of a sample from Vastmanland 12 1 4 33 of a sample from Uppsala 7 8 4 51 of a sample from Gothenburg 7 0 3 43 of a sample from Norrbotten 6 8 5 73 of a sample from Skane 6 6 15 228 of a sample from Stockholm 6 3 3 48 of a sample from Sydnorrland 6 3 2 32 of a sample from Vasterbotten 6 3 2 32 of a sample from Orebro 5 9 3 51 of a sample from Varmland Dalarna 5 4 2 37 of a sample from Ostra Gotaland and 5 1 2 39 of a sample from southeastern Sweden Kalmar Gotland Kronoberg and Blekinge They did not find any instance of N Tat in their samples from Jonkoping 0 28 Malmo 0 29 Halland 0 34 or Vastra Gotaland 0 75 33 N1a1a M178 Edit The subclade N M178 Phylogenetics 3 is defined by the presence of markers M178 and P298 N M178 has higher average frequency in Northern Europe than in Siberia reaching frequencies of approximately 60 among Finns and approximately 40 among Latvians Lithuanians amp 35 among Estonians Derenko 2007harvnb error no target CITEREFDerenko2007 help and Lappalainen 2008harvnb error no target CITEREFLappalainen2008 help Miroslava Derenko and her colleagues noted that there are two subclusters within this haplogroup both present in Siberia and Northern Europe with different histories The one that they labelled N3a1 first expanded in south Siberia and spread into Northern Europe Meanwhile the younger subcluster which they labelled N3a2 originated in south Siberia probably in the Baikal region Derenko 2007 harv error no target CITEREFDerenko2007 help N M178 was also found in two Na Dene speaking Tli chǫs in North America 61 Neolithic samples from Baikal area have yielded plenty of yDNA N specimens and one sample from Fofonovo Buryatia 5000 4000 BC is among the first Tat samples in the ancient record 59 Earliest samples of N1a1a L708 were found in Trans Baikal brn008 N1a1a1 L708 brn003 N1a1a1a1 M2126 between 8 000 and 6 000 YBP Downstream samples were found in Yakutia N4b2 N1a1a1a1a Z1979 and Krasnoyarsk Krai kra001 N1a1a1a1a L392 between 5 000 and 4 000 YBP 62 63 N1a2 F1008 L666 Edit N1a2a M128 and N1a2b B523 P43 are estimated to share a most recent common ancestor in N1a2 F1008 L666 approximately 8 600 95 CI 7 500 lt gt 9 800 years before present 1 9 200 years before present 64 or 9 314 95 CI 7 419 lt gt 11 264 years before present 3 At least three of six tested male specimens from the Early Neolithic ceramic using hunter gatherer of approximately 7200 6200 years ago layer at the Shamanka archaeological site near the southern end of Lake Baikal have been found to belong to N1a2 L666 55 N1a2a M128 Edit Haplogroup N M128 Possible place of originAsiaAncestorN1a2 F1008 L666 DescendantsF710 F1998Defining mutationsM128Highest frequenciesManchus 2 5 Liaoning 3 45 3 9 Jilin 0 0 Koreans 1 1 Liaoning 2 4 Jilin 2 0 2 5 Gyeongsang 1 2 Jeolla 1 1 Chungcheong 0 9 Seoul 0 3 Xibe 1 0 Han 0 89 Shanxi 1 83 Henan 1 53 Gansu 1 46 Hebei 1 41 Shaanxi 1 40 Tianjin 1 38 Shandong 1 17 Beijing 1 14 Inner Mongolia 1 13 Heilungjiang 1 12 Liaoning 1 12 Fujian 1 12 Anhui 0 93 Jilin 0 86 Ningxia 0 82 Jiangsu 0 81 Yunnan 0 79 Hubei 0 77 Zhejiang 0 73 Taiwan 0 70 Sichuan 0 54 Hunan 0 52 Chungqing 0 51 Guizhou 0 51 Guangdong 0 45 Hainan 0 43 Xinjiang 0 43 Shanghai 0 36 Jiangxi 0 34 Guangxi 0 23 Qinghai 0 18 Mongolians 0 7 Liaoning 1 9 Horqin 0 3 Ulaanbaatar 0 0 Japanese 0 3 Tokushima 3 5 Ibaraki 2 0 Hiroshima 1 3 Nagoya 1 0 Osaka 0 2 Tokyo 0 0 Shizuoka 0 0 Yamaguchi 0 0 Kazakhs 0 1 Khoja 1 9 Baiuly 0 6 Uysun 0 4 This subclade is defined by the presence of the marker M128 Phylogenetics 4 N M128 was first identified in a sample from Japan 1 23 4 3 and in a sample from Central Asia and Siberia 1 184 0 5 in a preliminary survey of worldwide Y DNA variation 51 Subsequently it has been found with low frequency in some samples of the Manchu people Sibe people Evenks Koreans Han Chinese Hui Tibetans Vietnamese Bouyei people Kazakhs Uzbeks Uyghurs Salars Tu Mongols the Buzava tribe of Kalmyks 29 Khakas and Komis 16 A number of a Han Chinese an Ooled Mongol a Qiang and a Tibetan were found to belong to a sister branch or branches of N M128 under paragroup N F1154 65 A neolithic sample brn002 5 940 BP in Trans Baikal was discovered to be an early offshoot upstream of N M128 66 62 As a genetic testing result of Yelu clan a royal family of the Liao Dynasty and Khitan descents it was found to belong to N F1998 a downstream of N M128 N1a2b P43 Edit Haplogroup N P43 Phylogenetics 5 is defined by the presence of the marker P43 It has been estimated to be approximately 4 000 to 5 500 years old TMRCA 4 510 years 64 TMRCA 4 700 95 CI 3 800 lt gt 5 600 ybp 1 or 4 727 95 CI 3 824 lt gt 5 693 years before present 3 It has been found very frequently among Northern Samoyedic peoples speakers of Ob Ugric languages and northern Khakassians and it also has been observed with low to moderate frequency among speakers of some other Uralic languages Turkic peoples Mongolic peoples Tungusic peoples and Siberian Yupik people The highest frequencies of N P43 are observed among north west Siberian populations 92 35 38 16 in a sample of Nganasan 78 7 9 67 18 in a sample of Enets 78 21 27 31 in a sample of Khants 75 44 59 16 in a sample of Tundra Nenets 69 29 42 3 in another sample of Nenets 60 15 25 12 in a sample of Mansi 57 64 112 11 in another sample of Khants 54 27 50 3 in another sample of Nganasan 45 40 89 16 in a sample of Forest Nenets 38 18 47 68 in a third sample of Khants and 25 7 28 12 in a fourth sample of Khants In Europe the N P43 types have their highest frequency of 20 among Volga Uralic populations The extreme western border of the spread of N P43 is Finland where this haplogroup occurs only at marginal frequency 0 4 Yet N P43 is quite frequent among Vepsas 17 9 a small Finnic population living in immediate proximity to Finns Karelians and Estonians 16 Haplogroup N P43 also has been observed with very high frequency 26 29 89 7 of a sample from the settlement of Topanov and 19 22 86 4 of a sample from the settlement of Malyi Spirin in samples of Kachins a Turkic speaking ethnic group or territorial subgroup of the Khakas people from Shirinsky District of northern Khakassia 9 There appears to be a cline through the Sagai another Turkic speaking ethnic group that is now considered to be a constituent of the Khakas people with 46 2 55 119 of Sagai sampled from Ust Es Esino Ust Chul and Kyzlas settlements of Askizsky District of central Khakassia belonging to haplogroup N P43 vs only 13 6 11 81 of Sagai sampled from Matur Anchul Bol shaya Seya and Butrakhty settlements of Tashtypsky District of southern Khakassia belonging to this haplogroup 9 However other researchers samples of Khakas people have exhibited only moderate frequencies of N P43 or potential N P43 Derenko et al 2006 examined a sample of Khakassians n 53 collected in the settlements of Askiz Shirinsk Beisk and Ordzhonikidzevsk districts of Khakass Republic and found that 15 of them 28 3 belonged to N LLY22g xTat 19 Rootsi et al 2007 examined a sample of Khakas n 181 and found that 31 of them 17 1 belonged to N P43 16 Ilumae et al 2016 retested 174 of the individuals in this sample and found that 27 of them 15 5 belonged to the N B478 Asian northern Samoyedic subclade of N P43 and 2 of them 1 1 belonged to the N L1419 European Volga Finnic and Chuvash subclade of N P43 for a total of 29 16 7 N P43 3 Haplogroup N P43 forms two distinctive subclusters of STR haplotypes Asian and European the latter mostly distributed among Finno Ugric speaking peoples and related populations Rootsi et al 2006 N1a2b1 B478 Edit The TMRCA of N B478 has been estimated to be 3 007 95 CI 2 171 lt gt 3 970 years before present 3 It is one of the most prevalent Y DNA haplogroups among indigenous populations of northwestern Siberia 69 0 29 42 Nenets 50 0 25 50 Nganasan 22 2 12 54 Dolgan from Taymyr 7 0 3 43 Selkup 1 6 1 63 Ob Ugrian It is also quite prevalent among populations of Central Siberia Southern Siberia and Mongolia 17 9 17 95 Tuvan 15 5 27 174 Khakas 13 0 6 46 Tozhu Tuvans 28 8 7 2 23 Shor 8 3 2 24 Even 8 2 5 61 Altaian 5 3 3 57 Evenk 5 0 19 381 Mongol 4 9 3 61 Sart Kalmak partial descendants of Oirat Mongols in Kyrgyzstan 28 4 2 9 216 Yakut 2 1 1 47 Torgut Mongolia 28 1 4 1 69 Derbet Kalmykia 28 0 9 1 111 Buryat A geographically outlying member has been found in a sample of Chuvash 1 114 0 88 3 Karafet et al 2018 observed N P63 which appears to be roughly phylogenetically equivalent to N B478 in 91 2 31 34 Nganasan 63 8 30 47 Tundra Nenets 42 7 35 82 Forest Nenets 14 0 8 57 Dolgan 7 0 9 129 Selkup 3 3 3 91 Evenk 2 7 2 75 Mongol 2 6 2 78 Komi 2 5 2 80 Buryat and 2 0 2 98 Altai Kizhi 6 This haplogroup was not observed in samples of Yukaghir 0 10 Koryak 0 11 Teleut 0 40 Ket 0 44 Yakut 0 62 or Khanty 0 165 populations 6 N1b F2930 Edit Haplogroup N1b has been predominantly found in the Yi people a Tibeto Burman speaking ethnic group in southwestern China who originated from ancient Qiang tribes in northwestern China 54 However it also has been found in people all over China and in some samples of people from Poland Belarus Russia Mongolia Korea Japan Vietnam Cambodia Bhutan and India N2 Y6503 Edit N2 Y6503 FGC28528 B482 FGC28394 Y6584 a primary branch of haplogroup N M231 is now represented mainly by a subclade N FGC28435 that has spread probably some time in the first half of the second millennium CE 69 and that has been found in individuals from Serbia Croatia Bosnia and Herzegovina Montenegro and Turkey Istanbul 70 69 N Y7310 or N F14667 subsumes N FGC28435 and likewise probably descends from a common ancestor who has lived some time in the first half of the last millennium However members of N Y7310 xFGC28435 exhibit a greater geographic range including an individual from Rostov Oblast of Russia and a Romanian Hungarian individual with ancestry from Suceava Bukovina 1 Other branches of N P189 include members from Turkey 1 Russia Moscow Oblast 1 France Charente Maritime 1 and England Devon 1 71 The most recent common ancestor of all the aforementioned extant N P189 lineages has been estimated to be 4 900 95 CI 5 700 lt gt 4 100 years before present 1 An archaeological specimen attributed to the Botai culture of northern Kazakhstan and dated to the latter half of the fourth millennium BCE belongs to N P189 being basal to present day European members of N P189 72 1 Lineages that belong to N Y6503 xP189 and are only distantly related with a time to most recent common ancestor estimated to be greater than 10 000 years before present 1 to the aforementioned members of N P189 have been found in an individual from the present day Altai Republic 1 and probably also in an archaeological specimen attributed to the Iron Age Mezocsat culture of what is now Hungary approx 2 900 years before present 73 and in an archaeological specimen attributed to the Kitoi culture of ceramic using foragers of the area around Lake Baikal approx 6 700 years before present 72 Ancient peoples Edit A sample excavated at the Houtaomuga site in the Yonghe neighborhood of Honggangzi Township Da an Jilin China dating back to 7430 7320 years ago Phase II of the Early Neolithic has been found to belong to Y DNA haplogroup N and mtDNA haplogroup B4c1a2 This sample is autosomally identical with the Neolithic Amur River Basin populations of which Nivkh people are the closest modern representative As the paper detected this ancestry in terminal Pleistocene USR1 specimen in Alaska it is therefore postulated that there was gene flow from Amur to America of a population belonging to a hypothetical Chukotko Kamchatkan Nivkh linguistic family 60 N has also been found in many samples of Neolithic human remains exhumed from Liao civilization in northeastern China and in the circum Baikal area of southern Siberia 74 It is suggested that yDNA N reached southern Siberia from 12 14 kya From there it reached southern Europe 8 10kya 52 Phylogeny EditPhylogenetic tree Edit In the following tree the nomenclature of three sources is separated by slashes ISOGG Tree 10 December 2017 ver 12 317 NO M214 N M231 Page91 M232 M2188 N1 Z4762 CTS11499 L735 M2291 N1a L729 N Z1956 N Y149447 China Shaanxi 1 N1a1 M46 Page70 Tat N1a1a M178 N1a1a1 F1419 N1a1a1a L708 N1a1a1a1 P298 M2126 China Urumqi Kashgar Prefecture Turpan Aksu Prefecture Xianyang Jincheng Kaifeng Qiqihar 64 N1a1a1a1a L392 N1a1a1a1a1 CTS10760 N1a1a1a1a1a CTS2929 VL29 Found with high frequency among Lithuanians Latvians Estonians northwestern Russians Swedish Saami Karelians Nenetses Finns and Maris moderate frequency among other Russians Belarusians Ukrainians and Poles and low frequency among Komis Mordva Tatars Chuvashes Dolgans Vepsa Selkups Karanogays and Bashkirs 3 N1a1a1a1a1a1 Z4908 N Y46443 N Y46443 Russia Moscow Oblast 1 N BY33095 Russia Samara Oblast 1 N1a1a1a1a1a1a L550 S431 N L550 Sweden Kronoberg County 1 N Y9454 Sweden Vastra Gotaland County 1 Orebro County 1 Finland 1 Russia 1 N Y20911 Finland Western Finland Province 1 Southern Finland Province 1 N Y7795 N Y7795 Sweden Norrbotten County 1 Sodermanland County 1 N Y29766 Norway Hedmark 1 N Y20918 Sweden Ostergotland County 1 Vasterbotten County 1 Finland Western Finland Province 1 N Y28771 N Y61225 Sweden Sodermanland County 1 Uppsala County 1 N Y30126 N Y30126 Sweden Ostergotland County 1 N Y29764 N Y29764 Sweden Stockholm County 1 N Y30123 Sweden Vasterbotten County 1 Finland 1 N S9378 N S9378 Sweden Vastra Gotaland County 1 N S18447 Sweden Sodermanland County 1 Uppsala County 1 N Y36282 N Y36282 Finland Southern Finland Province 1 Estonia Ida Virumaa 1 N BY21957 Poland Kujawsko pomorskie 1 Sweden Stockholm County 1 Russia Pskov Oblast 1 Finland Southern Finland Province 1 N FGC14542 N FGC14542 Finland Eastern Finland Province 1 N BY21938 Norway Hedmark 1 Sweden Dalarna County 1 N Y17113 United Kingdom Suffolk 1 Scotland 1 Canada Manitoba 1 Norway Vestfold 1 Buskerud 1 Sweden Vastra Gotaland County 1 N Y4341 N BY21874 Sweden Sodermanland County 1 Finland 1 N Y4338 N Y4338 N Y4339 Sweden medieval Sigtuna 1 N Y12104 N Y12104 Sweden Ostergotland County 1 N Y12103 Finland Western Finland Province 1 Sweden 1 Norway Hedmark 1 N Y19111 N Y57577 Sweden Skane County 1 N Y22774 Finland Western Finland Province 1 N Y5611 N Y5611 England 1 N Y21546 Sweden Stockholm County 1 Vastmanland County 1 N F1983 Sweden Gavleborg County 1 Russia Lipetsk Oblast 1 N Y10932 N Y85136 Sweden Uppsala County 1 N Y10931 Russia 1 N1a1a1a1a1a1a1 L1025 B215 Highest frequency among Lithuanians significant in Latvians and Estonians and lesser frequency in Belorussians Ukrainians South West Russians and Poles With exception of Estonians L1025 has highest share among N M231 clades in previously mentioned populations Also observed in Finland and Sweden with sporadic instances in Norway Germany Netherlands United Kingdom the Azores Czech Republic and Slovakia N L1025 Russia Kursk Oblast 1 N BY30389 Sweden Vasternorrland County 1 Finland Western Finland Province 1 N Y13982 N Y13982 Portugal Azores 1 N Y31236 Lithuania Marijampole County 1 Vilnius County 1 N A11940 N Y140872 Sweden Sodermanland County 1 Norrbotten County 1 Finland Southern Finland Province 1 N Y143451 Russia Bashkortostan 1 N Y5580 N Y93996 Lithuania Siauliai County 1 Poland Podlaskie 1 N BY158 Russia Voronezh Oblast 1 Smolensk Oblast 1 Tatarstan 1 Belarus Vitebsk Region 1 Lithuania Vilnius County 1 Siauliai County 1 Panevezys County 1 Poland Podlaskie 1 Ukraine Poltava Oblast 1 Kazakhstan Jambyl Region 1 N Z16975 N VL69 Belarus Minsk Region 1 Russia Bryansk Oblast 1 Kazakhstan Kostanay Region 1 N Z16976 N Z16976 Belarus Grodno Region 1 Ukraine Khmelnytskyi Oblast 1 N Y13475 Poland 1 Lithuania 1 N Y21578 Lithuania Kaunas County 1 Telsiai County 1 Russia Smolensk Oblast 1 N Y6129 Poland Warminsko mazurskie 1 Lithuania 1 N Y19113 Poland Warminsko mazurskie 1 Lithuania Taurage County 1 N Y134492 Belarus Grodno Region 1 Minsk Region 1 Mogilev Region 1 Lithuania 1 United States Illinois 1 N L551 N L551 Lithuania Vilnius County 1 N Y15251 Lithuania Alytus County 1 Poland Podlaskie 1 N Y46313 Latvia 1 N Y86578 Russia Belgorod Oblast 1 N Y14152 N BY21911 Poland 1 Latvia Kraslava District 1 Ukraine Kyiv Oblast 1 Finland Southern Finland Province 1 N Y13979 Lithuania 1 Russia Ryazan Oblast 1 Germany 1 N Y4706 N Y4706 Sweden Stockholm County 1 Sodermanland County 1 Vastra Gotaland County 1 Germany Lower Saxony 1 Finland Southern Finland Province 1 Russia Tatarstan 1 N A705 Sweden Kalmar County 1 Ostergotland County 1 N BY21893 Poland Wielkopolskie 1 N Y139030 Sweden Vasterbotten County 1 Norway Ostfold 1 N Y183040 Russia Vologda Oblast 1 Tatarstan 1 N Y4707 Finland Western Finland Province 1 Aland 1 Southern Finland Province 1 Eastern Finland Province 1 Oulu Province 1 N Z16981 N A2358 England 1 Finland 1 Latvia Daugavpils aprinkis 1 N CTS8173 Estonia Laane Virumaa 1 N BY32524 Estonia Jarvamaa 1 Finland Oulu Province 1 N FGC39882 Lithuania Telsiai County 1 N A11470 Russia Tyumen Oblast 1 Lithuania Panevezys County 1 Finland Southern Finland Province 1 Netherlands South Holland 1 North Brabant 1 N Y15922 Finland Southern Finland Province 1 Estonia Ida Virumaa 1 Parnumaa 1 Latvia Valmiera 1 Liepaja 1 Talsu aprinkis 1 Russia Pskov Oblast 1 Poland Pomorskie 1 N Y6075 Poland Malopolskie 1 Mazowieckie 1 Ukraine Lviv Oblast 1 Slovakia 1 Czech Republic Moravian Silesian Region 1 United States New Jersey 1 N Y11882 N Y11882 Russia Tatarstan 1 N ZS11617 Russia Yaroslavl Oblast 1 Lithuania 1 N Y24601 Latvia 1 N Y94659 Lithuania 1 Belarus Minsk Region 1 N Y32725 N FT96305 Latvia Kraslava District 1 Estonia Viljandimaa 1 N Y33333 Ukraine Sumy Oblast 1 Belarus Brest Region 1 N1a1a1a1a1a2 CTS9976 N L1022 N Y19098 N Y19098 Sweden Vasternorrland County 1 N A12258 Finland Eastern Finland Province 1 N BY117178 Finland Eastern Finland Province 1 N Y5004 N Y7300 N A17632 N Y128024 Sweden Ostergotland County 1 N A16017 N A16017 Estonia Raplamaa 1 N A16526 N FT216144 Finland Western Finland Province 1 N Y95406 Estonia Tartumaa 1 Russia Leningrad Oblast 1 N Y7297 Finland Western Finland Province 1 Southern Finland Province 1 Lapland Province 1 N Y15813 N Y15813 Finland Western Finland Province 1 N Y49008 Finland Western Finland Province 1 Oulu Province 1 N Y46886 Finland Western Finland Province 1 N Y15812 N A14187 Finland Western Finland Province 1 Estonia Laanemaa 1 N Y24617 Finland Western Finland Province 1 Sweden Dalarna County 1 Russia Kursk Oblast 1 N Y23576 N Y23576 Finland Eastern Finland Province 1 N Y15615 N BY100801 Sweden Dalarna County 1 Finland Western Finland Province 1 N A17838 Finland Western Finland Province 1 Southern Finland Province 1 Sweden Stockholm County 1 N Y23179 Finland Western Finland Province 1 Oulu Province 1 N Y5005 N Y22106 N Y47789 Finland Western Finland Province 1 N Y79341 Finland Western Finland Province 1 Sweden Vastra Gotaland County 1 Varmland County 1 N Y10756 N A13656 Finland Western Finland Province 1 Lapland Province 1 Sweden Dalarna County 1 N PH2196 N CTS11122 Finland Eastern Finland Province 1 N A17277 Finland Western Finland Province 1 Southern Finland Province 1 N PH547 Finland Lapland Province 1 Eastern Finland Province 1 Southern Finland Province 1 Sweden Vasterbotten County 1 Norrbotten County 1 N Y5003 N Y5003 Estonia Hiiumaa 1 Finland Southern Finland Province 1 United Kingdom Westminster 1 N BY22001 Estonia Laanemaa 1 Finland Western Finland Province 1 Sweden Norrbotten County 1 N BY6007 Russia Lipetsk Oblast 1 N Y132182 Sweden Varmland County 1 Estonia Viljandimaa 1 N Y20917 Sweden Kronoberg County 1 Finland Western Finland Province 1 Southern Finland Province 1 N Y24502 United Kingdom Scottish Borders 1 Calderdale 1 Kirklees 1 N Y18420 Finland Southern Finland Province 1 Western Finland Province 1 N Z35267 Finland Western Finland Province 1 Aland Province 1 Southern Finland Province 1 Estonia Parnumaa 1 N Y6599 Finland Eastern Finland Province 1 Oulu Province 1 Southern Finland Province 1 Estonia Jogevamaa 1 Hiiumaa 1 Russia Tula Oblast 1 N Y24000 N Y24001 Sweden Vasterbotten County 1 Norway Troms 1 N A17082 Finland Western Finland Province 1 Southern Finland Province 1 Estonia 1 N Y16503 Finland Western Finland Province 1 Southern Finland Province 1 Eastern Finland Province 1 Oulu Province 1 Sweden Gavleborg County 1 N BY6010 United States Virginia 1 N CTS3451 N CTS3451 Russian 1 N Y3667 N BY33087 N BY33087 Finland Southern Finland Province 1 N BY33088 Finland Eastern Finland Province 1 Russia Novgorod Oblast 1 N CTS657 N CTS657 Finland 1 Russia Republic of Karelia 1 Novgorod Oblast 1 N BY70437 Finland Eastern Finland Province 1 N BY6024 Finland Eastern Finland Province 1 N Y45925 Russia Republic of Karelia 1 N Y26750 N Y26750 Russia Arkhangelsk Oblast 1 N A16653 Finland Eastern Finland Province 1 N PH3568 Finland Oulu Province 1 Eastern Finland Province 1 N1a1a1a1a1b PH1266 Y28526 F4134 N Y46746 Russia 1 N Y32732 N Y32732 Russia Saint Petersburg 1 N Y192174 N Y32731 Russia Komi Republic 1 Sweden 1 N1a1a1a1a1c B479 Nanai 3 Ulchi 40 N1a1a1a1a2 Z1936 CTS10082 Found with high frequency among Finns Vepsa Karelians Swedish Saami northwestern Russians Bashkirs and Volga Tatars moderate frequency among other Russians Komis Nenetses Ob Ugrians Dolgans and Siberian Tatars and low frequency among Mordva Nganasans Chuvashes Estonians Latvians Ukrainians and Karanogays 3 N1a1a1a1a2a1c PH3340 Y13850 N1a1a1a1a2a1c1 L1034 N Y28538 N Y28538 Russia Khantia Mansia 1 N L1032 Russia Khantia Mansia 1 Kazakhstan East Kazakhstan Region 1 N L1442 Hungary 75 N FT12605 Russia Lipetsk Oblast 1 Greece Arkadia 1 N Y23732 Russia Bashkortostan 1 N Y24222 N Y24222 Russia Tatarstan 1 N Y62987 Russia Bashkortostan 1 Samara Oblast 1 N1a1a1a1a2a1c2 Y24361 N Y24361 N Y24360 Russia Tatarstan 1 N1a1a1a1a2a Z1934 N Y159520 N Y159520 Russia Tambov Oblast 1 N BY184755 Russia Novgorod Oblast 1 Voronezh Oblast 1 Moscow 1 N Y18421 N Y18421 Russia Tambov Oblast 1 N Y19110 N Y180247 N Y180247 Russia Tatarstan 1 N FT52835 Russia Tula Oblast 1 Moscow 1 N Y19108 N Y19108 Russia Tatarstan 1 Kirov Oblast 1 N Y19453 N Y19453 Russia Tatarstan 1 N Y19451 Finland Western Finland Province 1 Russia Republic of Karelia 1 Tver Oblast 1 N Z1928 CTS2733 N YP6091 N YP6091 Russia Irkutsk Oblast 1 N YP6094 N Y129131 N Y129131 Russia Kostroma Oblast 1 N A25107 Russia Kirov Oblast 1 HGDP Russian 1 N YP6092 N YP6092 Russia Vologda Oblast 1 N B195 N B195 Russia Sverdlovsk Oblast 1 N Y62142 Russia Republic of Karelia 1 Arkhangelsk Oblast 1 N1a1a1a1a2a Z1925 N Z1925 Sweden Norrbotten County 1 N Y29767 Sweden Norrbotten County 1 N Y62904 Finland Western Finland Province 1 Oulu Province 1 N1a1a1a1a2a2a1a1 Z1926 N Y20920 N Y20920 Finland Western Finland Province 1 Norway Nord Trondelag 1 N Y21699 Finland Western Finland Province 1 Southern Finland Province 1 N Z1927 N Y22108 Finland Eastern Finland Province 1 Southern Finland Province 1 Western Finland Province 1 Sweden Stockholm County 1 Orebro County 1 N Z1933 N CTS4329 N Y22091 N Y22091 Norway Nordland 1 Finland Lapland Province 1 N Y47623 N Y47623 Finland Lapland Province 1 N Y106419 Norway Finnmark 1 N Y31247 N Y31247 Russia Tver Oblast 1 N Y31249 N Y90283 Finland Lapland Province 1 N Y31244 Finland Western Finland Province 1 Eastern Finland Province 1 N YP6269 N YP6269 Finland Western Finland Province 1 N Y151660 N Y151660 Finland Eastern Finland Province 1 N BY149208 Sweden Norrbotten County 1 N CTS8565 N BY18114 Finland Eastern Finland Province 1 N BY30394 Finland Eastern Finland Province 1 Russia Udmurt Republic 1 N Y30513 N Y30513 Finland Southern Finland Province 1 N Y29759 N Y29759 Finland Lapland Province 1 N Y29758 Sweden Norrbotten County 1 N Z4998 N Z4998 Finland Southern Finland Province 1 N FGC65190 Finland Southern Finland Province Eastern Finland Province N Y18414 Finland Western Finland Province N Y20910 Finland Western Finland Province N BY194138 Finland Southern Finland Province N Y28547 Finland Eastern Finland Province N BY22141 Finland Western Finland Province Eastern Finland Province United States Washington N FT5834 Finland Western Finland Province Southern Finland Province N BY190112 Finland Western Finland Province Southern Finland Province N Y19097 Finland Eastern Finland Province Southern Finland Province Western Finland Province Oulu Province N CTS3223 Finland Southern Finland Province Eastern Finland Province Western Finland Province Oulu Province Lapland Province Sweden Norrbotten County Vasterbotten County Dalarna County Varmland County Skane County Russia Leningrad Oblast N VL62 Russia Altai Krai 1 Kostroma Oblast 1 Estonia Harjumaa 1 Finland 1 N VL62 Russia Chelyabinsk Oblast 1 Finland 1 N VL60 N VL60 Russia Kurgan Oblast 1 N Y63781 Russia Vladimir Oblast 1 Arkhangelsk Oblast 1 N VL72 N VL72 Russia Republic of Karelia 1 N BY30470 Finland Western Finland Province 1 N Y20915 Finland Eastern Finland Province 1 N Z1939 N Y132561 N Y132565 Finland Eastern Finland Province 1 N Y152012 N Y152012 Finland 1 N Y152010 Russia Leningrad Oblast 1 N Z2445 N Z35031 Finland Eastern Finland Province Western Finland Province Sweden Vastra Gotaland County Vastmanland County N BY28931 N Y125841 Finland Eastern Finland Province 1 Western Finland Province 1 N Y11631 Finland Western Finland Province 1 Eastern Finland Province 1 Southern Finland Province 1 Oulu Province 1 Russia Leningrad Oblast 1 Sweden Norrbotten County 1 N CTS7189 N BY142665 Finland Eastern Finland Province 1 N Y37149 Finland Eastern Finland Province 1 N Y23568 Finland Eastern Finland Province 1 N Y80226 Finland Eastern Finland Province 1 N FT20730 Finland Eastern Finland Province 1 Russia Republic of Karelia 1 N BY62666 Finland Eastern Finland Province 1 Norway Oslo 1 United States Virginia 1 Arkansas 1 N Y24218 N Y24218 Finland Lapland Province 1 Oulu Province 1 Eastern Finland Province 1 N Y24217 Finland Western Finland Province 1 Eastern Finland Province 1 Russia Bashkortostan 1 N BY22038 Finland Eastern Finland Province 1 Southern Finland Province 1 Western Finland Province 1 N Y13974 Finland Southern Finland Province 1 Eastern Finland Province 1 Oulu Province 1 Western Finland Province 1 N Y135981 Finland Eastern Finland Province 1 Oulu Province 1 Southern Finland Province 1 Western Finland Province 1 Norway Finnmark 1 N Z4747 N Y17790 Finland Eastern Finland Province 1 Southern Finland Province 1 Western Finland Province 1 N Z1941 N BY22090 Finland Southern Finland Province 1 Eastern Finland Province 1 N Y21575 Finland Western Finland Province 1 Southern Finland Province 1 Eastern Finland Province 1 Oulu Province 1 Lapland Province 1 Russia Leningrad Oblast 1 Moscow 1 Tatarstan 1 N Z1940 Finland Western Finland Province 1 Southern Finland Province 1 Eastern Finland Province 1 Oulu Province 1 Lapland Province 1 Russia Leningrad Oblast 1 Sweden Varmland County 1 N1a1a1a1a3 B197 Y16323 N1a1a1a1a3a F4205 Found with high frequency among Buryats 3 and Tsaatans 28 moderate frequency among Karanogays 3 Tuvans 3 Todjins 28 and Mongols 3 28 and low frequency among Altaians 3 Siberian Tatars 3 Kazakhs 3 Evenks 3 Crimean Tatars 3 Karakalpaks 3 Uzbeks 3 and Ukrainians 3 N F4205 China Inner Mongolia Gansu Xinjiang Henan etc 64 N Y16221 N Y16221 China Inner Mongolia 1 N Y16220 N Y16220 Ukraine Luhansk Oblast 1 N F22331 Turkey Mersin 1 Poland Malopolskie 1 Kazakhstan Pavlodar Regionca 1680 ybp 1 N Y63966 Kazakhstan 1 Turkey 1 Uzbekistan 1 N Y226011 N Z35331 China Ordos City Haidong Chengdu 64 N B199 Russia Buryatia 1 China Huasai from Hulunbuir 64 N FT411781 China Inner Mongolia 1 N Y16312 F2288 N Y16312 Uzbekistan 1 China Xibo from Shenyang Chaoyang Tangshan Beijing Nanjing Chifeng Xianyang Tacheng Prefecture 64 N Y16320 Kazakhstan 1 China Inner Mongolia 1 N1a1a1a1a3b B202 Found with high frequency among Chukchis 3 Koryaks 3 and Siberian Eskimos 3 N1a1a1a1b M2019 M2118 Estonia 1 76 China Hami Yan an Xi an Luliang Changzhi Xilingol League Chifeng Cangzhou Songyuan 64 N M2058 China Shandong Liaoning Henan Inner Mongolia Gansu etc 64 1 N M2016 China esp Xinjiang and Inner Mongolia 64 N M1993 N FT411801 China Inner Mongolia 1 N1a1a1a1b1 M2038 M1995 N M1932 Yakutia Yakuts 1 Even 1 N M1991 N M1988 Yakutia Yakuts 1 N Y25011 Yakutia Yakut 1 Evenki 1 N1a1a1a1b2 A9408 China Hebei Shandong Henan etc 64 Lebanon 53 3 N Y70200 China 1 Shaanxi Shanxi Shandong etc 64 N Y60223 Korean 1 China Shandong 64 Hebei 64 Henan 64 Liaoning 64 Jiangsu 64 Shaanxi 1 64 Shanxi 64 etc N PH1612 China Yulin Shangqiu Dezhou Tangshan Shenyang 64 N A9407 A9411 China Ili Kazakh Autonomous Prefecture 64 N A9416 Hungary Szabolcs Szatmar Bereg 1 Croatia Zadar County 1 Russia Chuvash Republic 1 N PH1896 Hungary Borsod Abauj Zemplen 1 Turkey Hatay 1 76 China Xinjiang Shandong Anhui Heilongjiang Hebei Ningxia Guizhou 64 N1a1a1a2 B211 Y9022 Udmurt 3 Komi 3 Chuvash 3 Ob Ugrians 3 Mari 3 Mordva 3 Altaian 3 Belarusian 3 Karanogay 3 Karelian 3 Bashkir 3 Tatar 76 Russian 3 76 Khakas 3 N1a1a1a2a B181 N Y182299 Russia Kirov Oblast etc 1 N Y23788 Russia Bashkortostan Komi Republic etc 1 N1a1a1a2b Y23181 N Y23183 Russia Tatarstan Mordovia Penza Oblast 1 N Y143277 Russia Tatarstan Bashkortostan 1 N Y24317 N Y24317 xB187 India Andhra Muslim 1 76 N1a1a1b B187 Khakas 3 1 Shors 3 53 Altaians 3 Tuvinians 3 Tozhu Tuvan 28 Tatar 3 Bashkir 3 N1a1a2 Y23747 Japan Sado Island 76 N1a1a2a Y23749 Japan 3 Aichi 1 Hokkaidō 1 N1a1a2b Y125664 N Y125664 Shanghai 1 N MF16376 N1a1a2b1 MF38607 Anhui 1 Hunan 1 N1a1a2b2 F22150 Hebei 1 Suzhou 64 N FT281705 China Shandong Liaoning etc 64 N MF200125 China Linyi Changchun 64 N MF43738 China Tonghua Handan Anyang Qingdao Weinan Suzhou Shanghai Shaoxing Chuxiong Yi Autonomous Prefecture 64 N MF82671 N MF124520 China Henan Zhejiang Anhui Shanxi etc 64 N MF58064 F19130 China Hulunbuir 64 Daur 1 64 Oroqen 1 77 Hinggan League 64 N MF15288 MF15344 China esp Jiangsu but also Henan Fujian Shanghai Heilongjiang 1 etc 64 South Korea 1 N MF55680 China Hebei Beijing Hubei etc 64 N MF37603 China Jiangsu etc 64 N F21121 China Shigatse Tibetan 78 1 Tai an 64 N MF48201 South Korea 1 China Linfen Baoji 64 N F1360 N F1360 China Shaanxi 1 N1a2 F1008 L666 N F1101 N F1101 China Shandong 1 N F1154 N F1154 China Liaoning 1 N Y23741 N Y23741 China 1 N1a2a M128 N M128 Japan Fukui 1 N Y23738 Vietnam 1 N CTS1350 N CTS1350 China Liaoning 1 Tianjin 1 N F1998 N F1998 China Beijing Han 1 Henan 1 Japan Kumamoto 1 N MF1633 China Guangdong 1 Zhejiang 1 N MF41795 Korea North Jeolla Province 1 N Y71703 N Y71703 Japan Saitama 1 Hyōgo 1 N Y173843 N Y173843 South Korea 1 N Y174089 China Shandong 1 N1a2b B523 P43 N1a2b Y126204 VL67 Z35079 BY29083 N VL67 Z35079 N1a2b1 B478 P63 Nenets Nganasans Dolgans Tuvans Todzhins 28 Khakasses Shorians Evens Altaians Selkups Evenks Mongols Sart Kalmak 28 Torgut 28 Derbet 28 Buryat Yakuts Ob Ugrians Chuvashes N1a2b1a B168 Evens N1a2b1b B169 N1a2b1b1 B170 Nenets Khanty Mansi Autonomous Okrug Inner Mongolia N1a2b1b2 B175 Tuvinians Mongols Evenks Yakuts Tomsk Oblast N1a2b3 B525 Turkey Tatars Bashkirs Kazakhs Mongols Xinjiang Kalmyk 28 Mongolian Torgut 28 Slovakia Bulgaria 1 Ukrainians Belarusians Russians N B525 Afghanistan Arab N BY173686 Russia Voronezh Oblast 1 N VL83 Turkey 1 N Y136502 Russia Tatarstan 1 Bulgaria Dobrich 1 N Y37153 N Y37153 Russia Tatarstan 1 N BY29131 N BY29131 Turkey Konya 1 Slovakia Zilina Region 1 N BY30476 Russia Tatarstan 1 Penza Oblast 1 N1a2b2 FGC10872 Y3195 N1a2b2a FGC10847 Y3185 L1419 Vepsas Maris Russians Arkhangelsk Oblast Komis Perm Krai Komi Republic Ob Ugrians Chuvashes Tatars Bashkirs Karelians Western Finland Province Tuvans Buryats Khakasses Nganasans Asian Eskimos N1a2b2b Y23786 N1a2b2b Mansis N1a2b2b1 B528 Y24384 Udmurts Komis Khanties Tatars Asian Eskimos Kirov Oblast Perm Krai Medny Island N1b F2905 N1b1 CTS582 China esp Jiangsu Yunnan Hebei Shandong Shanxi Heilongjiang 64 N1b1a Y6374 Z8029 N1b1a1 CTS7324 Beijing 1 N1b1a2 L727 N1b1a2 L727 Beijing 1 N1b1a2a L732 Belarus 71 N1b1a2a1 F839 China esp Jiangsu 64 Shandong 64 Zhejiang 64 Shanghai 1 64 Henan 64 N F18335 China Shandong 1 64 Beijing 64 N F16160 China Jiangsu 1 64 Shandong 64 Xinjiang Han 1 N Y137601 China esp Zhejiang 1 64 Hebei 64 Liaoning 64 N1b1a2a2 Y15972 N F21018 MF105942 Found all over China but especially in Zhejiang Sichuan Anhui Shanghai Guangdong Shandong Henan and Jiangsu 64 N Y62279 China esp Fujian 1 64 and Guangdong 64 but also Sichuan 1 64 Zhejiang 64 etc Taiwan 64 N MF155949 China esp Zhejiang but also Anhui Jiangxi Hubei Hunan Guangdong and Beijing 64 N L733 Hong Kong 1 79 mainland China esp Shandong Shanxi Zhejiang Beijing Jiangsu and Sichuan 64 N Y154812 China Shanxi 1 64 N Y16106 China esp Shandong Jiangsu Liaoning Anhui 64 Poland 71 N Y232856 China esp Henan 64 but also Shaanxi 1 64 Guangdong 64 etc N Y15965 Poland Pomorskie 1 N1b1b Y23789 CTS4309 Iraq 71 N1b1b Y23789 Beijing Han 1 Fujian 1 N1b1b1 Y60861 Guangxi 1 N1b2 M1819 N M1897 CTS12473 F1173 China 71 Russian Federation 71 N M1897 ancient DNA from Pingliangtai Henan ca 4 063 95 CI 3 974 lt gt 4 151 ybp 1 N M1845 N M1845 China Sichuan 1 Shanghai 1 N M1928 N M1928 Sichuan Han 1 N Y125475 N Y63516 China Chongqing 1 Korea South Pyongan Province 1 South Chungcheong Province 1 N Y193396 China Ningxia 1 Singapore 1 N CTS4714 N CTS4714 China Naxi 1 Yunnan Hui 1 N F2407 N Y24191 N Y24191 China Shandong 1 N Y24193 N Y24193 China Hebei 1 N Y24190 China Henan 1 Japan Hokkaido 1 N M1877 N M1877 Shigatse Tibetan 1 N F1486 Chongqing 1 N F1486 United Kingdom Telugu 1 80 Mongolia 1 N M1812 N F1260 N F1260 Hubei Han 1 N Y62067 N Y62067 Guangdong 1 N Y62132 Hong Kong 1 79 China 1 N M1823 N M1823 Chongqing 1 N M1811 N M1811 Beijing Han 1 Guangxi 1 N Y24355 N Y24355 China 1 Macau 1 Ho Chi Minh City Kinh 1 N Y64234 Guangdong 1 N2 Y6503 N2 Y6503 Altai Republic 1 N2a P189 2 N2a1 Y6516 N2a1 Y6516 N2a1a Y7310 N2a1a Y7310 Romania Hungarian from Suceava 1 N2a1a1 Y7313 N2a1a1 Y7313 N2a1a1a BY35494 Russia Rostov Oblast 1 N2a1a1b FGC28435 N2a1a1b FGC28435 Turkey Istanbul Serbia Montenegro Pluzine Bosnia and Herzegovina Republika Srpska Croatia 1 N2a1a1b1 FGC28483 Serbia 1 N2a2 Y111068 N2a2a FT352925 France Charente Maritime 1 Turkey 1 N2a2b Y101945 United Kingdom Devon 1 Russia Moscow Oblast 1 History of phylogenetic nomenclature Edit Main article Conversion table for Y chromosome haplogroups Prior to 2002 there were in academic literature at least seven naming systems for the Y Chromosome Phylogenetic tree This led to considerable confusion In 2002 the major research groups came together and formed the Y Chromosome Consortium YCC They published a joint paper that created a single new tree that all agreed to use Later a group of citizen scientists with an interest in population genetics and genetic genealogy formed a working group to create an amateur tree aiming at being above all timely The table below brings together all of these works at the point of the landmark 2002 YCC Tree This allows a researcher reviewing older published literature to quickly move between nomenclatures YCC 2002 2008 Shorthand a b g d e z h YCC 2002 Longhand YCC 2005 Longhand YCC 2008 Longhand YCC 2010r Longhand ISOGG 2006 ISOGG 2007 ISOGG 2008 ISOGG 2009 ISOGG 2010 ISOGG 2011 ISOGG 2012N LLY22g 12 VIII 1U 25 Eu16 H5 F N N N1 N1 N M128 12 VIII 1U 25 Eu16 H5 F N1 N1 N1a N1a N P63 12 VIII 1U 25 Eu16 H5 F N2 N2a N1b1 N1b1 N TAT 12 VIII 1I 26 Eu13 H5 F N3 N3 N1c N1c N M178 16 VIII 1I 26 Eu14 H5 F N3a M178 N1c1 N1c1 N P21 16 VIII 1I 26 Eu14 H5 F N3a1 N3a1 N1c1a N1c1a Sources The following research teams per their publications were represented in the creation of the YCC Tree a Jobling amp Tyler Smith 2000 and Kaladjieva 2001 b Underhill et al 2000 g Hammer 2001 d Karafet et al 2001 e Semino 2000 z Su 1999 h Capelli 2001 Unreliable mutations SNPs and UEPs The b2 b3 deletion in the AZFc region of the Y chromosome appears to have occurred independently on at least four different occasions Therefore this deletion should not be taken as a unique event polymorphism defining this branch of the Y chromosome tree ISOGG 2012 Links to genetics concepts Edit genetic genealogy Genetic history of Europe Haplogroup Haplotype Human Y chromosome DNA haplogroup molecular phylogeny Paragroup Subclade Y chromosome haplogroups in populations of the world Y DNA haplogroups by ethnic group Y DNA haplogroups in populations of East and Southeast Asia Y DNA haplogroups in populations of Europe Y DNA N subclades Edit N M231 Y DNA backbone tree EditFootnotes Edit In Karafet et al 2010References Edit a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx by bz ca cb cc cd ce cf cg ch ci cj ck cl cm cn co cp cq cr cs ct cu cv cw cx cy cz da db dc dd de df dg dh di dj dk dl dm dn do dp dq dr ds dt du dv dw dx dy dz ea eb ec ed ee ef eg eh ei ej ek el em en eo ep eq er es et eu ev ew ex ey ez fa fb fc fd fe ff fg fh fi fj fk fl fm fn fo fp fq fr fs ft fu fv fw fx fy fz ga gb gc gd ge gf gg gh gi gj gk gl gm gn go gp gq gr gs gt gu gv gw gx gy gz ha hb hc hd he hf hg hh hi hj hk hl hm hn ho hp hq hr hs ht hu hv hw hx hy hz ia ib ic id ie if ig ih ii ij ik il im in io ip iq ir is it iu iv iw ix iy iz ja jb jc jd je jf jg jh ji jj jk jl jm jn jo jp jq jr js jt ju jv jw jx jy jz ka kb kc kd ke kf kg kh ki kj kk kl km kn ko kp kq kr ks kt ku kv kw kx ky kz la lb lc ld le lf lg lh li lj lk ll lm ln lo lp lq lr ls lt lu lv lw lx ly lz ma mb mc md me mf mg mh mi mj mk ml mm mn mo mp mq mr ms mt mu mv mw mx my mz na nb nc nd ne nf ng nh ni nj nk nl nm nn no np nq nr ns nt nu nv nw nx ny nz oa ob oc od oe of og oh oi oj ok ol om on oo op oq or os ot ou ov ow ox oy oz pa pb pc pd pe pf pg ph pi pj pk pl pm pn po pp pq pr ps pt pu pv pw px py pz qa qb qc qd qe qf qg qh qi qj qk ql qm qn qo qp qq qr qs qt qu qv qw qx qy qz ra rb rc rd re rf rg rh ri rj rk rl rm rn ro rp rq rr rs rt ru rv rw rx ry rz sa sb sc sd se sf sg sh si sj sk sl sm sn so sp sq sr ss st su sv sw sx sy sz ta tb tc td te tf tg th ti tj tk tl tm tn to tp tq tr ts tt tu tv tw YFull Haplogroup YTree v6 05 11 at 25 September 2018 a b c Poznik GD Xue Y Mendez FL Willems TF Massaia A Wilson Sayres MA et al June 2016 Punctuated bursts in human male demography inferred from 1 244 worldwide Y chromosome sequences Nature Genetics 48 6 593 599 doi 10 1038 ng 3559 PMC 4884158 PMID 27111036 a b c d e f g h i j k l m n o p q r s t u v w x y z aa ab ac ad ae af ag ah ai aj ak al am an ao ap aq ar as at au av aw ax ay az ba bb bc bd be bf bg bh bi bj bk bl bm bn bo bp bq br bs bt bu bv bw bx by bz Ilumae et al 2016 a b c d ISOGG 2016 Y DNA Haplogroup N and its Subclades 2016 22 August 2016 Rootsi et al 2006 a b c d e f g h Karafet TM Osipova LP Savina OV Hallmark B Hammer MF November 2018 Siberian genetic diversity reveals complex origins of the Samoyedic speaking 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Europe European Journal of Human Genetics 15 2 204 211 doi 10 1038 sj ejhg 5201748 PMID 17149388 Sirak K Fernandes D Cheronet O Harney E Mah M Mallick S et al March 2020 Human auditory ossicles as an alternative optimal source of ancient DNA Genome Research 30 3 427 436 doi 10 1101 gr 260141 119 PMC 7111520 PMID 32098773 Wen B Xie X Gao S Li H Shi H Song X et al May 2004 Analyses of genetic structure of Tibeto Burman populations reveals sex biased admixture in southern Tibeto Burmans American Journal of Human Genetics 74 5 856 865 doi 10 1086 386292 PMC 1181980 PMID 15042512 Xue Y Zerjal T Bao W Zhu S Shu Q Xu J et al April 2006 Male demography in East Asia a north south contrast in human population expansion times Genetics 172 4 2431 2439 doi 10 1534 genetics 105 054270 PMC 1456369 PMID 16489223 Websites ISOGG 2012 Y DNA Haplogroup Tree 2012 McDonald D 2004 Macdonald Y Haplogroups of the World PDF Archived from the original PDF on 2004 07 28 Retrieved 2009 08 29 Sources for conversion tables Edit Capelli Cristian Wilson James F Richards Martin Stumpf Michael P H et al February 2001 A Predominantly Indigenous Paternal Heritage for the Austronesian Speaking Peoples of Insular Southeast Asia and Oceania The American Journal of Human Genetics 68 2 432 443 doi 10 1086 318205 PMID 11170891 Hammer Michael F Karafet Tatiana M Redd Alan J Jarjanazi Hamdi et al 1 July 2001 Hierarchical Patterns of Global Human Y Chromosome Diversity Molecular Biology and Evolution 18 7 1189 1203 doi 10 1093 oxfordjournals molbev a003906 PMID 11420360 Jobling Mark A Tyler Smith Chris 2000 New uses for new haplotypes Trends in Genetics 16 8 356 62 doi 10 1016 S0168 9525 00 02057 6 PMID 10904265 Kaladjieva Luba Calafell Francesc Jobling Mark A Angelicheva Dora et al February 2001 Patterns of inter and intra group genetic diversity in the Vlax Roma as revealed by Y chromosome and mitochondrial DNA lineages European Journal of Human Genetics 9 2 97 104 doi 10 1038 sj ejhg 5200597 PMID 11313742 Semino O Passarino G Oefner PJ Lin AA et al 2000 The Genetic Legacy of Paleolithic Homo sapiens sapiens in Extant Europeans A Y Chromosome Perspective Science 290 5494 1155 1159 Bibcode 2000Sci 290 1155S doi 10 1126 science 290 5494 1155 PMID 11073453 Su Bing Xiao Junhua Underhill Peter Deka Ranjan et al December 1999 Y Chromosome Evidence for a Northward Migration of Modern Humans into Eastern Asia during the Last Ice Age The American Journal of Human Genetics 65 6 1718 1724 doi 10 1086 302680 PMC 1288383 PMID 10577926 Underhill PA Shen P Lin AA Jin L et al November 2000 Y chromosome sequence variation and the history of human populations Nature Genetics 26 3 358 361 doi 10 1038 81685 PMID 11062480 S2CID 12893406 Further reading Edit This section needs expansion You can help by adding to it December 2012 ISOGG 2006 Y DNA Haplogroup Tree 2006 ISOGG 2007 Y DNA Haplogroup Tree 2007 ISOGG 2008 Y DNA Haplogroup Tree 2008 ISOGG 2009 Y DNA Haplogroup Tree 2009 ISOGG 2010 Y DNA Haplogroup Tree 2010 ISOGG 2011 Y DNA Haplogroup Tree 2011 ISOGG 2018 Y DNA Haplogroup N and its Subclades YFull YFull Experimental YTree ISOGG 2019 2020 https docs google com spreadsheets d 1ju7oNjHjMrgMUB1xXmr0EaaL RctJJ8FreUPM2DzuBY edit gid 692817756Phylogenetics Edit The b2 b3 deletion in the AZFc region of the human Y chromosome is a characteristic of Haplogroup N M231 haplotypes This deletion however appears to have occurred independently on four different occasions Therefore this deletion should not be thought as a unique event polymorphism contributing to the definition of this branch of the Y chromosome tree ISOGG 2012 This table shows historic names for N M46 AKA N Tat from peer reviewed literature YCC 2002 2008 Shorthand N M46 N TATJobling and Tyler Smith 2000 12Underhill 2000 VIIIHammer 2001 1IKarafet 2001 26Semino 2000 Eu13Su 1999 H5Capelli 2001 FYCC 2002 Longhand N3 YCC 2005 Longhand N3YCC 2008 Longhand N1cYCC 2010r Longhand N1c This table shows historic names for N M178 from peer reviewed literature YCC 2002 2008 Shorthand N M178Jobling and Tyler Smith 2000 16Underhill 2000 VIIIHammer 2001 1IKarafet 2001 26Semino 2000 Eu14Su 1999 H5Capelli 2001 FYCC 2002 Longhand N3a YCC 2005 Longhand M178YCC 2008 Longhand N1c1YCC 2010r Longhand N1c1 This table shows historic names for N M128 from peer reviewed literature YCC 2002 2008 Shorthand N M128Jobling and Tyler Smith 2000 12Underhill 2000 VIIIHammer 2001 1UKarafet 2001 25Semino 2000 Eu16Su 1999 H5Capelli 2001 FYCC 2002 Longhand N1YCC 2005 Longhand N1YCC 2008 Longhand N1aYCC 2010r Longhand N1a This branch is sometimes called N1b in early trees External links Edit Wikimedia Commons has media related to Haplogroup N of Y DNA Spread of Haplogroup N from The Genographic Project National Geographic N North Eurasian YDNA Project at FamilyTreeDNA N Y DNA Haplogroup Project at FamilyTreeDNA N1c1 Y DNA Haplogroup Project at FamilyTreeDNA Y chromosome haplogroup N dispersals from south Siberia to Europe Rurikid Dynasty DNA Project at FamilyTreeDNA Russian Nobility DNA Project at FamilyTreeDNA Retrieved from https en wikipedia org w index php title Haplogroup N M231 amp oldid 1145235277, wikipedia, wiki, book, books, library,

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