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Haplogroup I-M438

Haplogroup I-M438, also known as I2 (ISOGG 2019), is a human DNA Y-chromosome haplogroup, a subclade of Haplogroup I-M170. Haplogroup I-M438 originated some time around 26,000–31,000 BCE. It originated in Europe and developed into several main subgroups : I2-M438*, I2a-L460, I2b-L415 and I2c-L596.[2] The haplogroup can be found all over Europe and reaches its maximum frequency in the Dinaric Alps (Balkans) via founder effect.[4] Examples of basal I-M438* have been found in males from Crete and Sicily .[5]

Haplogroup I-M438
Possible time of origin28–33,000 years ago[1]
Possible place of originSouth-Eastern or Eastern Europe.
AncestorI-M170
DescendantsI-L460, I-L1251
Defining mutationsM438/P215/S31
Highest frequenciesI2a1a: Sardinia[2]

I2a1b: Bosnia and Herzegovina,[3]

I2a2: Britain, Germany, and Sweden[2]

Origin & prehistoric presence

Haplogroup I2a was the most frequent Y-DNA among western European mesolithic hunter gatherers (WHG) belonging to Villabruna Cluster. A 2015 study found haplogroup I2a in 13,500 year old remains from the Azilian culture (from Grotte du Bichon, modern Switzerland).[6] Subclades of I2a1 (I-P37.2), namely I-M423 and I-M26 have been found in remains of Western European Hunter-Gatherers dating from 10,000 to 8,000 years before present respectively.[7]

In a 2015 study published in Nature, the remains of six individuals from Motala ascribed to the Kongemose culture were successfully analyzed. With regards to Y-DNA, two individuals were ascribed to haplogroup I2a1b, one individual was ascribed to haplogroup I2a1, and one individual was ascribed to haplogroup I2c.[8]

Subclades of I-L460

I-P37.2

The I-P37.2+, also known as I2a1a (ISOGG 2019) (The subclade divergence for I-P37.2 occurred 10.7±4.8 kya. The age of YSTR variation for the P37.2 subclade is 8.0±4.0 kya.[2] It is the predominant version of I2 in Eastern Europe.[9] The I2a is further made up by sub-groups I-M26, I-M423, I-L1286, I-L880.

I-L158

Haplogroup I-M26 (or M26) I2a1a1a (ISOGG 2019).

Haplogroup I-L158 (L158, L159.1/S169.1, M26) accounts for approximately 40% of all patrilines among the Sardinians.[10][11] It is also found at low to moderate frequency among populations of the Pyrenees (9.5% in Bortzerriak, Navarra; 9.7% in Chazetania, Aragon; 8% in Val d'Aran, Catalunya; 2.9% in Alt Urgell, Catalunya; and 8.1% in Baixa Cerdanya, Catalunya) and Iberia, and it has been found in 1.6% of a sample of Albanians living in the Republic of North Macedonia[12] and 1.2% (3/257) of a sample of Czechs.[13] The age of YSTR variation for the M26 subclade has been calculated at 8.0±4.0 kya.[2]

I-L178

I-L178 is very rare, but has been found in two persons from Germany and one from Poland. The age of YSTR variation for the M423 subclade is 8.8±3.6 kya.[1]

I2a-L621
 
The approximate frequency and variance distribution of haplogroup I-P37 clusters, ancestral "Dnieper-Carpathian" (DYS448=20) and derived "Balkan" (DYS448=19: represented by a single SNP I-PH908), in Eastern Europe per O.M. Utevska (2017).

I2a1a2b-L621 is typical of the Slavic populations, being highest in Southeastern European regions of Bosnia-Herzegovina and South Croatia (>45%),[3][14][15] in Bosniaks (43.53-52.17%), Croats (37.7-69.8%), and Serbs (36.6-42%), because of which is often called "Dinaric".[16] It has the highest variance and also high concentration in Eastern Europe (Ukraine, Southeastern Poland, Belarus).[17] According to YFull YTree it formed 11,400 YBP and had TMRCA 6,500 YBP, while its main subclades lineage is I-CTS10936 (6,500-5,600 YBP) > I-S19848 (5,600 YBP) > I-CTS4002 (5,600-5,100 YBP) > I-CTS10228 (5,100-3,400 YBP) > I-Y3120 (3,400-2,100 YBP) > I-Y18331 (2,100 YBP) / I-Z17855 (2,100-1650 YBP) / I-Y4460 (2,100 YBP) / I-S17250 (2,100-1,850 YBP) > I-PH908 (1,850-1,700 YBP).[18]

Older research considered that the high frequency of this subclade in the South Slavic-speaking populations to be the result of "pre-Slavic" paleolithic settlement in the region. Peričić et al. (2005) for instance place its expansion to have occurred "not earlier than the YD to Holocene transition and not later than the early Neolithic".[2][3][19][20] However the prehistoric autochthonous origin of the haplogroup I2 in the Balkans is now considered as out of date,[nb 1] as already Battaglia et al. (2009) observed highest variance of the haplogroup in Ukraine, and Zupan et al. (2013) noted that it suggests it arrived with Slavic migration from the homeland which was in present-day Ukraine.[25] The research by O.M. Utevska (2017) concluded that the haplogroup STR haplotypes have the highest diversity in Ukraine, with ancestral STR marker result "DYS448=20" comprising "Dnieper-Carpathian" cluster, while younger derived result "DYS448=19" comprising the "Balkan cluster" which is predominant among the South Slavs.[17] This "Balkan cluster" also has the highest variance in Ukraine, which indicates that the very high frequency in the Western Balkan is because of a founder effect.[17] Utevska calculated that the STR cluster divergence and its secondary expansion from the middle reaches of the Dnieper river or from Eastern Carpathians towards the Balkan peninsula happened approximately 2,860 ± 730 years ago, relating it to the times before Slavs, but much after the decline of the Cucuteni–Trypillia culture.[17] However, STR-based calculations give overestimated dates,[26][27] and more specifically, the "Balkan cluster" is represented by a single SNP, I-PH908, known as I2a1a2b1a1a1c in ISOGG phylogenetic tree (2019), and according to YFull YTree it formed and had TMRCA approximately 1,850-1,700 YBP (2nd-3rd century AD).[18]

It is considered that I-L621 could have been present in the Cucuteni–Trypillia culture,[28] but until now was mainly found G2a and non-I2-L621 clades,[29][30] and another clade I2a1a1-CTS595 was present in the Baden culture of the Chalcolithic Carpathian Basin.[28][31][32] Although it is dominant among the modern Slavic peoples on the territory of the former Balkan provinces of the Roman Empire, until now it was not found among the samples from the Roman period and is almost absent in contemporary population of Italy.[16] It was found in the skeletal remains with artifacts, indicating leaders, of Hungarian conquerors of the Carpathian Basin from the 9th century, part of Western Eurasian-Slavic component of the Hungarians.[16][28][33] According to Pamjav et al. (2019) and Fóthi et al. (2020), the distribution of ancestral subclades like of I-CTS10228 among contemporary carriers indicates a rapid expansion from Southeastern Poland, is mainly related to the Slavs and their medieval migration, and the "largest demographic explosion occurred in the Balkans".[16][34] The earliest archeogenetic sample until now is Sungir 6 (~900 YBP) near Vladimir, Russia which belonged to the I-S17250 > I-Y5596 > I-Z16971 > I-Y5595 > I-A16681 subclade,[35][36] as well I-CTS10228 and I-Y3120 subclades were found in two Viking samples from Sweden (VK53) and Ukraine (VK542) with predominantly Slavic ancestry of which the second belongs to Gleb Svyatoslavich (11th century).[37]

I-M223

Haplogroup I-M223 aka I2a1b1 (ISOGG 2019), formerly I2a2a (ISOGG 2014). The age of YSTR variation for the I-M223 subclade has been variously estimated as 13.2±2.7 kya,[2] 12.3±3.1 kya.[1], 14.6 kya[38] and 14.6±3.8 kya (Rootsi 2004). I-M223 has a peak in Germany and another in the northeast of Sweden, but also appears in Romania/Moldova, Russia, Greece, Italy and around the Black Sea.[39] Haplogroup I-M223 has been found in over 4% of the population only in Germany, the Netherlands, Belgium, Denmark, Scotland, and England (excluding Cornwall) – also the southern tips of Sweden and Norway in Northwest Europe; the provinces of Normandy, Maine, Anjou, and Perche in northwestern France; the province of Provence in southeastern France; the regions of Tuscany, Umbria, and Latium in Italy; Moldavia and the area around Russia's Ryazan Oblast and Mordovia in Eastern Europe. Of historical note, both haplogroups I-M253 and I-M223 appear at a low frequency in the historical regions of Bithynia and Galatia in Turkey. Haplogroup I-M223 also occurs among approximately 1% of Sardinians.

I-M284

Haplogroup I2a1b1a1a (ISOGG 2019) or I-M284, has been found almost exclusively amongst the populations of the United Kingdom and Ireland suggesting that it may have arisen amongst the Ancient Britons, with a most recent common ancestor (MRCA) who lived about 3,100 years BP.[40] The presence of this subclade "provides some tentative evidence of ancient flow with eastern areas that could support the idea that the [late Celtic] La Tene culture was accompanied by some migration."[41]

Where it is found in those of predominately Irish descent, with Gaelic surnames, it may suggest an ancestor who arrived in Ireland during prehistory, from Celtic Britain.[41] For example, I-M284 includes many males with the surnames McGuinness and McCartan, who have a single, historically-recorded male ancestor in the 6th century; thus it is unlikely to be the result of subsequent migration from Britain to Ireland.[41] Some subclades of I-M284 that are atypical of Ireland are relatively common in continental Europe,[41] which also supports a point of origin east of Ireland.

I-CTS10057

Continentals. Mother Haplogroup for group I-Z161 (Continental 1 and 2) and I-L701 group (Continental 3). Around 10.000 years old.

I-Z161

Haplogroup I2a1b1a2b (ISOGG 2019). Z161+ defines the I2 Continental clade 1 and 2. Its age is estimated around 7,000 years old. It is mainly found in North Europe, especially in Denmark, Germany, the Netherlands, and England. In Northwest Sicily it can also be found; this is believed to be due to remnants of a Norman settlement.

I-L701

Called Continental 3. Continental 3 has a wide distribution. Found in Central Europe from Germany, Austria to Poland, Romania and Ukraine, but also in lower frequencies in Greece, Italy, France, Spain, England, Ireland, and Armenia. It may have been disseminated in part by the Goths. It is nearly absent from Scandinavia and Scotland.

I-M436

Subclades list

Up-to-date phylogenetic trees listing subclades of I can be found at Y-Full and FamilyTreeDNA

Haplogroup I
I1

I1a

I1b

I1c

I1d

I1e

I2

I2a

I2b

I2*


Subclades list


•I2 M438/P215/PF3853/S31 (16638804 A->G)
• •I2a L460/PF3647/S238 (7879415 A->C)
• • •I2a1 P37.2/PF4004 (14491684 T->C)
• • • •I2a1a CTS595 (6874115 C->T)
• • • • •I2a1a1 M26/PF4056 (21865821 G->A)
• • • • • •I2a1a1a CTS8968/PF4036 (18584762 T->C)
• • • • • • •I2a1a1a1 L672/S327 (22228628 T->A)
• • • • • • • •I2a1a1a1a L160/PF4013/S184
• • • • • • •I2a1a1a2 CTS6027 (16620529 C->G) w. Europeans
• • • • • • •I2a1a1a3 Z27395 (16681589 A->G)
• • • • • • • •I2a1a1a3a Z27410 (18891640 T->G)
• • • • • • • • •I2a1a1a3a1 Z27430 (15383072 T->C)
• • • • • • • • • •I2a1a1a3a1a Z27446 (14420039 G->A)
• • • • • • • • • • •I2a1a1a3a1a1 Z27447 (17445510 A->G)
• • • • • • • • • • • •I2a1a1a3a1a1a Z27452 (7346620 C->T) Sardinians
• • • • • • • • • • • •I2a1a1a3a1a1b Z27453 (22045753 C->A)
• • • • • • • • • • • • •I2a1a1a3a1a1b1 Z27456 (13885862 T->C) Sardinians
• • • • • •I2a1a1b Z27354 (7132292 T->C)
• • • • • • •I2a1a1b1 Z27400 (2833818 C->T) Sardinians
• • • • •I2a1a2 S21825 (19126655 G->A)
• • • • • •I2a1a2a L1286 (21778662 G->A)
• • • • • • •I2a1a2a1 L1287 (21970862 G->T)
• • • • • • • •I2a1a2a1a L233/S183 (14487362 G->A)
• • • • • • • • •I2a1a2a1a1 A417 (8846964 T->C) Brits
• • • • • • •I2a1a2a2 L880 (3436270 C->T) central Europeans
• • • • • •I2a1a2b L1294 (2887401 T->C) French
• • • • •I2a1a3 S2699 (14434372 C->T)
• • • •I2a1b M423 (19096091 G->A)
• • • • •I2a1b1 L161.1/S185.1 (22513718 C->T)
• • • • • •I2a1b1a L1498/Y4008 (18668472 C->T)
• • • • • • •I2a1b1a1 FGC7218/Y5280 (21354226 G->A) Irish
• • • • • • •I2a1b1a2 FGC14448/Y5450 (7158983 A->G) Irish
• • • • • • •I2a1b1a3 FGC7108/S2640 (14107847 G->A)
• • • • • • • •I2a1b1a3a FGC7197/S7703 (17494645 G->C)
• • • • • • • • •I2a1b1a3a1 S7714 (21345894 T->A)
• • • • • • • • • •I2a1b1a3a1a S8889 (4310132 A->G)
• • • • • • • •I2a1b1a3b S2742 (19440521 A->G)
• • • • • • • •I2a1b1a3c FGC7173/Y3729 (8472670 A->T)
• • • • • • • • •I2a1b1a3c1 FGC7156/Y4665 (2685333 T->C)
• • • • • • • • • •I2a1b1a3c1a FGC7218/Y5280 (21354226 G->A)
• • • • • • • • •I2a1b1a3c2 FGC14453/Y5456 (16637771 A->G)
• • • • • • •I2a1b1a4 A1150 (15543414 A->T)
• • • • • •I2a1b1b PF4135 (18981938 G->A) Brits
• • • • • •I2a1b1c CTS8849.2 (18236845 A->G)
• • • • • •I2a1b1d PF6316.2 (18181850 T->G)
• • • • •I2a1b2 L621/S392 (18760081 G->A)
• • • • • •I2a1b2a CTS4002 (15328797 C->A)
• • • • • • •I2a1b2a1 CTS10228 (9334357 A->C)
• • • • • • • •I2a1b2a1a S17250/YP204 (15531354 G->A)
• • • • • • • • •I2a1b2a1a1 Z16971 (6676628 G->C) Slovenians, Germans, Ukrainians
• • • • • • • • •I2a1b2a1a2 Y3548 (14856842 A->G) Sardinians
• • • • • • • • • •I2a1b2a1a2a Y4882 (21135222 G->A) Poles
• • • • • • • • •I2a1b2a1a3 A356/Z16983 (17558968 T->C)
• • • • • • • • • •I2a1b2a1a3a Y6651 (23792119 A->G) Czechs
• • • • • • • •I2a1b2a1b Y4460 (9028830 G->A)
• • • • • • • • •I2a1b2a1b1 Y3118 (23548545 T->C)
• • • • • • • • • •I2a1b2a1b1a CTS5579/S5054 (16378157 G->T) Finns
• • • • • • • •I2a1b2a1b V19.2 (2189,200 T->C)
• • • • • • • •I2a1b2a1c P61.2 (14482194 G->A)
• • •I2a2 M436/P214/PF3856/S33 (18747493 G->C)
• • • •I2a2a M223 (21717307 G->A)
• • • • •I2a2a1 CTS616 (6906332 G->C)
• • • • • •I2a2a1a Y3721 (7982615 C->T)
• • • • • • •I2a2a1a1 M284 (22750461..22750464 ACAA->del)
• • • • • • • •I2a2a1a1a L1195 (18865320 G->A)
• • • • • • • • •I2a2a1a1a1 L126/S165 (14901633 C->T)
• • • • • • • • • •I2a2a1a1a1a FGC20048/S7753/Y4171 (17603051 G->T)
• • • • • • • • • • •I2a2a1a1a1a1 FGC20065/Y4751 (18635722 A->G)
• • • • • • • • • • • •I2a2a1a1a1a1a Y4750 (23059262 C->G)
• • • • • • • • • • • • •I2a2a1a1a1a1a1 FGC20062/Y4753 (16910733 G->T) Irish, Scots
• • • • • • • • • • • • •I2a2a1a1a1a1a2 Y8599 Irish
• • • • • • • • • •I2a2a1a1a1b Y7190 (7987909 C->T) Scots
• • • • • • • • • •I2a2a1a1a1c F3878.2 (8752246 G->A)
• • • • • • • • •I2a2a1a1a2 L1193 (9448484 C->A)
• • • • • • • • • •I2a2a1a1a2a CTS4922 (15903939 T->C)
• • • • • • • • • • •I2a2a1a1a2a1 FGC14237/Y5996 (8292320 G->T) Irish
• • • • • • • • • •I2a2a1a1a2b CTS3792/S2380 (15183633 C->T)
• • • • • • •I2a2a1a2 Z2057 (4770006 T->C)
• • • • • • • •I2a2a1a2a L1229 (14937828 C->A)
• • • • • • • • •I2a2a1a2a1 Y3681 (22519059 T->C)
• • • • • • • • • •I2a2a1a2a1a Z2058 (5317533 T->C)
• • • • • • • • • • •I2a2a1a2a1a1 Z2054 (2980725 C->T)
• • • • • • • • • • • •I2a2a1a2a1a1a BY524/Y9443 (6371561 A->G)
• • • • • • • • • • • • •I2a2a1a2a1a1a1 L812/S391 (14850035 G->A)
• • • • • • • • • • • • • •I2a2a1a2a1a1a1a Y5308 (16820196 G->A)
• • • • • • • • • • • • •I2a2a1a2a1a1a2 Y10648 (8267867 C->G)
• • • • • • • • • • • •I2a2a1a2a1a1b Y7244 (8271590 C->T) Germans
• • • • • • • • • • • • •I2a2a1a2a1a1b1 P53.3 (14491649 T->C)
• • • • • • • • • • • • •I2a2a1a2a1a1b2 Y7243 (2911078 G->A)
• • • • • • • • • • • •I2a2a1a2a1a1c FGC15106/Y4334 (7845669 G->T)
• • • • • • • • • • • • •I2a2a1a2a1a1c1 FGC15128/Y4714 (15945966 G->C) Irish
• • • • • • • • • • • • •I2a2a1a2a1a1c2 Y4760 (15025945 A->T) Brits, Germans
• • • • • • • • • • • •I2a2a1a2a1a1d BY138 (2809424 A->T) Mexicans, English
• • • • • • • • •I2a2a1a2a2 S18331 (16449714 C->T) Brits
• • • • • • • • • •I2a2a1a2a2a L1230 (3436442 G->A) Brits
• • • • • • • •I2a2a1a2b Y7240 (2688254 T->G) English
• • • • • •I2a2a1b CTS10057 (19232160 C->T)
• • • • • • •I2a2a1b1 L702 (7629205 C->T)
• • • • • • • •I2a2a1b1a P78 (6740387 G->A)
• • • • • • • • •I2a2a1b1a1 S25733 (23595728 C->T)
• • • • • • • • • •I2a2a1b1a1a A427 (23281929 G->T)
• • • • • • • • • • •I2a2a1b1a1a1 S23612 (21826246 C->T) Brits, Italians, Germans
• • • • • • • • • • • •I2a2a1b1a1a1a Y5360 (23185624 G->T)
• • • • • • • • • • • •I2a2a1b1a1a1b S10702 (7822881 T->C)
• • • • • • • • • • •I2a2a1b1a1a2 Y5369 (23185624 G->T) Brits
• • • • • • • • •I2a2a1b1a2 Y7219 (8447173 C->A)
• • • • • • • • • •I2a2a1b1a2a Y7214 (4901002 C->A) Dutch
• • • • • • • • • •I2a2a1b1a2b Y8945 (4567154 G->A)
• • • • • • • •I2a2a1b1b L699 (2663920 A->G)
• • • • • • • • •I2a2a1b1b1 L704 (17595966 C->A)
• • • • • • • • • •I2a2a1b1b1a S12195 (9105096 C->T)
• • • • • • • • • • •I2a2a1b1b1a1 Y6973 (8430276 A->G)
• • • • • • • • •I2a2a1b1b2 Z26416 (18851267 G->A) Sardinians
• • • • • • • • •I2a2a1b1b3 PF6901 (17558585 C->G) Sardinians
• • • • • • • •I2a2a1b1c PF6896 (8904322 C->T) Brits, French
• • • • • • •I2a2a1b2 Z161 (2696497 C->G)
• • • • • • • •I2a2a1b2a L801/S390 (21763755 A->C)
• • • • • • • • • •I2a2a1b2a1 CTS1977 (14140273 G->A)
• • • • • • • • • • •I2a2a1b2a1a Y5282 (7982615 C->T)
• • • • • • • • • • • •I2a2a1b2a1a1 S8522 (3162610 T->C)
• • • • • • • • • • • • •I2a2a1b2a1a1a P95 (14869706 G->T) Poles, n.w. Europeans
• • • • • • • • • • • •I2a2a1b2a1a2 CTS1858 (14098206 G->T)
• • • • • • • • • • • • •I2a2a1b2a1a2a CTS10148 (19291083 A->T) African Americans
• • • • • • • • • • •I2a2a1b2a1b Y7152 (5852771 C->T)
• • • • • • • • • • •I2a2a1b2a1c BY526 or Y8935
• • • • • • • • • •I2a2a1b2a2 CTS6433 (16889964 T->C)
• • • • • • • • • • •I2a2a1b2a2a S2364 (23052606 A->G)
• • • • • • • • • • • •I2a2a1b2a2a1 FGC3618/S2361 (17355245 A->G)
• • • • • • • • • • • • •I2a2a1b2a2a1a Z78 (9154908 T->C)
• • • • • • • • • • • • • •I2a2a1b2a2a1a1 CTS8584
• • • • • • • • • • • • • • •I2a2a1b2a2a1a1a Z185 (22929384 T->C)
• • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1 Z180 (22065434 A->G)
• • • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1a L1198 (18405788 C->T))
• • • • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1a1 Z190 (17473966 G->T)
• • • • • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1a1a S434/Z79 (17147721 G->A) English
• • • • • • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1a1a1 Y5729 (14394460 C->T) English
• • • • • • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1a1a2 Y7682 (not yet reported)
• • • • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1a1b Y7280 (17305030 T->G)
• • • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1a2 FGC3617/S2368/Z166 (14010863 G->T)
• • • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1a3 P195.2 (22665262 A->G) Brits
• • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1b Y5748 (14106278 C->T)
• • • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1b1 Y7272 (19264274 G->A)
• • • • • • • • • • • • • • • •I2a2a1b2a1b1a1a1c Y7273 (16449864 A>G)
• • • • • • • • • • • • •I2a2a1b2a1b1a2 Y9161 (9154908 T->C)
• • • • • • • • • • • •I2a2a1b2a1b1b Y4925/ZS20 (23977120 A->C)
• • • • • • • • • • • • •I2a2a1b2a1b1b1 CTS661/L1272 (6931960 G->A)
• • • • • • • • • • • • • •I2a2a1b2a1b1b1a Y5717 (6931960 G->A)
• • • • • • • • • • • • •I2a2a1b2a1b1b2 FGC17399/Y4926 (23549293 G->A)
• • • • • • • • • • • • • •I2a2a1b2a1b1b2a S8104 (7432604 A->G)
• • • • • • • • • • • •I2a2a1b2a1b1c Y4955 (15362162 G->A)
• • • • • • • • • • • • •I2a2a1b2a1b1c1 Y5695 (14574229 T->C)
• • • • • • • • • • • • • •I2a2a1b2a1b1c1a Y7263 (7900806 C->A)
• • • • • • • • • • • • • • •I2a2a1b2a1b1c1a1 Y7265 (9147689 T->C)
• • • • • • • • • • • • • •I2a2a1b2a1b1c1b FGC20004/Y5692 (18993826 A->T)
• • • • • • • • • • • • •I2a2a1b2a1b1c2 Y10659 (4616653 A->G)
• • • • • • • • • • •I2a2a1b2a1b2 L1425 (14491835 C->T)
• • • • • • • • • • • •I2a2a1b2a1b2a CTS5332.2/PF7472.2 (16212441 G->A)
• • • • • • • • • • • •I2a2a1b2a1b2b Y4769 (18201094 A->G) Germans
• • • • • • • • • • •I2a2a1b2a1b3 Y7426 (18830768 A->G) English
• • • • • • • • • • •I2a2a1b2a1b4 S243/Z63 (14401486 C->T)
• • • • • • • • • • •I2a2a1b2a1b5 M3268.2/PF3292.2 (8519704 G->A) Germans
• • • • • • • • • • •I2a2a1b2a1b6 DF5.2/S191.2 (18393814 A->G) Brits
• • • • • • • • • • •I2a2a1b2a1b7 F3406.2 (23119516 G->A)
• • • • • • • • • •I2a2a1b2a2 L1290 (14623983 T->C) n. Europeans
• • • • • • • • • •I2a2a1b2a3 Y7202 (2913976 G->A) Germans
• • • • • • • •I2a2a1b2b L623 (16202490 A->T)
• • • • • • • •I2a2a1b2c CTS11871/S3673 (23326304 C->T) Brits, Germans
• • • • • • • •I2a2a1b2d Y5188 (7838639 G->A) Maltese
• • • • • • •I2a2a1b3 S12606 (9879942 T->G)
• • • • • • • •I2a2a1b3a CTS12640/S4904/ZS21 (28652639 C->T)
• • • • •I2a2a2 S9403/SK1254 (6742730 T->C)
• • • • • •I2a2a2a L1228 (15446045 G->C) w. Europeans
• • • • • •I2a2a2b Y6099 (7527993 G->A)
• • • •I2a2b L38/S154 (15668070 A->G)
• • • • •I2a2b1 L533/S295 (2887198 G->C) n.w. Europeans
• • • • •I2a2b2 S2606 (22527402 C->A)
• • • • • •I2a2b2a S2523 (14951410 C->T)
• • • • • • •I2a2b2a1 S24121 (22201497 C->A)
• • • • • • • •I2a2b2a1a S11558 (8491250 G->A)
• • • • • • • •I2a2b2a1b F780.2 (6384078 G->A)
• • • • •I2a2b3 M8990/S3846 (7534645 A->C)
• • • • • •I2a2b3a S2488 (12733783 T->A) English
• • • • • •I2a2b3b S4556 (14124389 A->G)
• • • • •I2a2b4 P15.2/PF3112.2 (3244026 C->T)
• •I2b L415/S435 (2888663 C->T) or L417/S332 (8426321 T->C) Germans, Italians
• •I2c L596/PF6907/S292 (14197631 G->A) or L597/S333 (18887888 T->A)
• • •I2c1 PF3892 (8487200 T->C)
• • • •I2c1a L1251 (2888598 C->T) Germans
• • • •I2c1b CTS4092 (15391894 G->A)
• • • • •I2c1b1 CTS7767.1 (17651573 C->A)
• • • • • •I2c1b1a PF6328 (21797244 C->A)
• • • • • • •I2c1b1a1 F2044 (15944600 T->A) Brits
• • • •I2c1c S6685 (14185048 G->C)
• • • • •I2c1c1 S6648 (14459289 T->A)
• • • • • •I2c1c1a FGC18548 (7380574 A->G) Sardinians
• • • • • •I2c1c1b S6716 (16173282 G->C)
• • • • • • •I2c1c1b1 S6622 (14264992 A->G)
• • • • • • • •I2c1c1b1a S6595 (21430083 G->A)
• • • • • • • • •I2c1c1b1a1 S6656 (17410728 G->C)
• • • • • •I2c1c1c S9234 (6512608 A->G)
• • •I2c2 PF3827 (22444389 T->A)
• • •I2c3 S6800 (16180130 G->A)

See also

Notes

  1. ^ The SNP I-P37 itself formed approximately 21,000 YBP and had TMRCA 18,400 YBP according to YFull YTree,[21] being too old and widespread as an SNP for argumentation of ancient autochthony or medieval migration as well the old research used outdated nomenclature. According to "I-P37 (I2a)" project at Family Tree DNA, the divergence at STR marker DYS448 20 > 19 is reported since 2007,[22] while the SNP which defines the STR Dinaric-South cluster, I-PH908, is reported since 2014.[23] The SNP I-PH908 at ISOGG phylogenetic tree is named as I2a1a2b1a1a1c,[24] while formed and had TMRCA approximately 1,800 YBP according to YFull.[18]

References

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  2. ^ a b c d e f g Rootsi S, Magri C, Kivisild T, Benuzzi G, Help H, Bermisheva M, et al. (July 2004). "Phylogeography of Y-chromosome haplogroup I reveals distinct domains of prehistoric gene flow in europe". American Journal of Human Genetics. 75 (1): 128–137. doi:10.1086/422196. PMC 1181996. PMID 15162323.
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  16. ^ a b c d Fóthi E, Gonzalez A, Fehér T, Gugora A, Fóthi Á, Biró O, Keyser C (2020). "Genetic analysis of male Hungarian Conquerors: European and Asian paternal lineages of the conquering Hungarian tribes". Archaeological and Anthropological Sciences. 12 (1). doi:10.1007/s12520-019-00996-0. We looked at 16 loci from 640 I2a-L621 samples in FTDNA’s I2a project database and found that 7 individuals were 2 genetic steps away the Karos samples, of whom 1 was a Hungarian from Kunszentmárton, 2 were Ukrainians, 1 was Lithuanian, 1 was Belarusian, 1 was Russian, and 1 was a German from Poland. Based on SNP analysis, the CTS10228 group is 2200 ± 300 years old. The group's demographic expansion may have begun in Southeast Poland around that time, as carriers of the oldest subgroup are found there today. The group cannot solely be tied to the Slavs, because the proto-Slavic period was later, around 300–500 CE ... The SNP-based age of the Eastern European CTS10228 branch is 2200 ± 300 years old. The carriers of the most ancient subgroup live in Southeast Poland, and it is likely that the rapid demographic expansion which brought the marker to other regions in Europe began there. The largest demographic explosion occurred in the Balkans, where the subgroup is dominant in 50.5% of Croatians, 30.1% of Serbs, 31.4% of Montenegrins, and in about 20% of Albanians and Greeks. As a result, this subgroup is often called Dinaric. It is interesting that while it is dominant among modern Balkan peoples, this subgroup has not been present yet during the Roman period, as it is almost absent in Italy as well (see Online Resource 5; ESM_5). ... Their genetic haplogroup, I2a-CTS10228, is widespread among Slavs, but it is only present in 7% of Caucasian peoples, namely among the Karachay ... As such, it appears that the I2a-CTS10228 haplogroup in the paternal lineage of the Karos leaders arises from a specific branch in the Northern Caucasus dating to about 400–500 CE. Its modern descendents live among the Karachay, Hungarians, and various other surrounding nationalities.
  17. ^ a b c d O.M. Utevska (2017). Генофонд українців за різними системами генетичних маркерів: походження і місце на європейському генетичному просторі [The gene pool of Ukrainians revealed by different systems of genetic markers: the origin and statement in Europe] (PhD) (in Ukrainian). National Research Center for Radiation Medicine of National Academy of Sciences of Ukraine. pp. 219–226, 302.
  18. ^ a b c "I-PH908 YTree v8.06.01". YFull.com. 27 June 2020. Retrieved 17 July 2020.
  19. ^ Marjanovic D, Fornarino S, Montagna S, Primorac D, Hadziselimovic R, Vidovic S, et al. (November 2005). "The peopling of modern Bosnia-Herzegovina: Y-chromosome haplogroups in the three main ethnic groups". Annals of Human Genetics. 69 (Pt 6): 757–763. doi:10.1111/j.1529-8817.2005.00190.x. PMID 16266413. S2CID 36632274.
  20. ^ Rębała K, Mikulich AI, Tsybovsky IS, Siváková D, Džupinková Z, Szczerkowska-Dobosz A, Szczerkowska Z (16 March 2007). "Y-STR variation among Slavs: evidence for the Slavic homeland in the middle Dnieper basin". Journal of Human Genetics. 52 (5): 406–414. doi:10.1007/s10038-007-0125-6. PMID 17364156.
  21. ^ "I-P37 YTree v8.06.01". YFull.com. 27 June 2020. Retrieved 17 July 2020.
  22. ^ "I2a Y-Haplogroup - Results: I2a2a-Dinaric". Family Tree DNA. Retrieved 11 November 2018. Ken Nordtvedt has split I2a2-M423-Dinaric into Din-N and Din-S. Din-N is older than Din-S. N=north of the Danube and S=south of the Danube River ... May 8, 2007: Dinaric I1b1 and DYS 448. DYS448 19 for S and 20 for N.
  23. ^ Bernie Cullen (22 August 2016). "Link to I-L621 tree showing major STR clusters (Updated)". i2aproject.blogspot.com. Blogger. Retrieved 3 April 2019.
  24. ^ "Y-DNA Haplogroup I and its Subclades - 2019-2020". ISOGG. 1 October 2019. Retrieved 17 July 2020.
  25. ^ Zupan A, Vrabec K, Glavač D (2013). "The paternal perspective of the Slovenian population and its relationship with other populations". Annals of Human Biology. 40 (6): 515–526. doi:10.3109/03014460.2013.813584. PMID 23879710. S2CID 34621779.
  26. ^ Šarac J, Šarić T, Havaš Auguštin D, Novokmet N, Vekarić N, Mustać M, et al. (November 2016). "Genetic heritage of Croatians in the Southeastern European gene pool-Y chromosome analysis of the Croatian continental and Island population". American Journal of Human Biology. 28 (6): 837–845. doi:10.1002/ajhb.22876. PMID 27279290. S2CID 25873634. It is important to stress that the proposed old age of the I2a1b-M423 and R1a1a1b1a*-M558 lineages obtained in previous studies (Battaglia et al., 2009; Peričić et al., 2005; Rootsi et al., 2004; Underhill et al., 2007, 2015) has been based on STR analysis (8 and 10 loci, respectively) and recent studies clearly indicate that the STR-based age calculations tend to yield overestimated dates (Batini et al., 2015; Hallast et al., 2015; Karmin et al., 2015).
  27. ^ Balanovsky O (May 2017). "Toward a consensus on SNP and STR mutation rates on the human Y-chromosome". Human Genetics. 136 (5): 575–590. doi:10.1007/s00439-017-1805-8. PMID 28455625. S2CID 3714493. While the reasons for the difference between genealogical and evolutionary Y-STR rates are thus partly understood, it remains unclear which rate to use. Many have applied the evolutionary rate, though quite a few have used the genealogical, or both, rates. Genetic genealogists generally apply the genealogical rate and criticize population-genetic studies for reporting (in their view) three-times overestimated ages ... The age of each haplogroup was also calculated using the STR genealogical rate and the STR evolutionary rate. Confidence intervals for the two STR-based ages (not shown on the plot) do not overlap. For example, the genealogical age of I2a-L621 (2200 ± 500 years) reaches the envelope age (from 2600 to 3100 ages), while the evolutionary age lies far beyond (9900 ± 2700 years). The observed pattern (Fig. 2a) clearly differs for haplogroups of different age classes. For ages less than 7000 years, the genealogical STR rate provides results consistent with or slightly underestimating the "true" ages, while the evolutionary rate results in three-fold overestimates. For ages between roughly 7000 and 15,000 years neither STR rate provides correct results. For haplogroups older than 15,000 years, the evolutionary rate estimates correctly or overestimates the "true" age.
  28. ^ a b c Neparáczki E, Maróti Z, Kalmár T, Maár K, Nagy I, Latinovics D, et al. (November 2019). "Y-chromosome haplogroups from Hun, Avar and conquering Hungarian period nomadic people of the Carpathian Basin". Scientific Reports. Nature Research. 9 (1): 16569. Bibcode:2019NatSR...916569N. doi:10.1038/s41598-019-53105-5. PMC 6851379. PMID 31719606. Hg I2a1a2b-L621 was present in 5 Conqueror samples, and a 6th sample form Magyarhomorog (MH/9) most likely also belongs here, as MH/9 is a likely kin of MH/16 (see below). This Hg of European origin is most prominent in the Balkans and Eastern Europe, especially among Slavic speaking groups. It might have been a major lineage of the Cucuteni-Trypillian culture and it was present in the Baden culture of the Calcholitic Carpathian Basin24 ... The identical I2a1a2b Hg-s of Magyarhomorog individuals appears to be frequent among high-ranking Conquerors, as the most distinguished graves in the Karos2 and 3 cemeteries also belong to this lineage.
  29. ^ Mathieson I, Alpaslan-Roodenberg S, Posth C, Szécsényi-Nagy A, Rohland N, Mallick S, et al. (March 2018). "The genomic history of southeastern Europe". Nature. 555 (7695): 197–203. Bibcode:2018Natur.555..197M. doi:10.1038/nature25778. PMC 6091220. PMID 29466330.
  30. ^ Gelabert P, Schmidt RW, Fernandes DM, Karsten JK, Harper TK, Madden GD, et al. (May 2022). "Genomes from Verteba cave suggest diversity within the Trypillians in Ukraine". Scientific Reports. Nature Research. 12 (1): 7242. doi:10.1038/s41598-022-11117-8. PMC 9068698. PMID 35508651.
  31. ^ Lipson M, Szécsényi-Nagy A, Mallick S, Pósa A, Stégmár B, Keerl V, et al. (November 2017). "Parallel palaeogenomic transects reveal complex genetic history of early European farmers". Nature. 551 (7680): 368–372. Bibcode:2017Natur.551..368L. doi:10.1038/nature24476. PMC 5973800. PMID 29144465.
  32. ^ Patterson N, Isakov M, Booth T, Büster L, Fischer CE, Olalde I, et al. (January 2022). "Large-scale migration into Britain during the Middle to Late Bronze Age". Nature. 601 (7894): 588–594. Bibcode:2022Natur.601..588P. doi:10.1038/s41586-021-04287-4. PMC 8889665. PMID 34937049. S2CID 245509501.
  33. ^ Maróti Z, Neparáczki E, Schütz O, Maár K, Varga GI, Kovács B, et al. (July 2022). "The genetic origin of Huns, Avars, and conquering Hungarians". Current Biology. 32 (13): 2858–2870.e7. doi:10.1016/j.cub.2022.04.093. PMID 35617951. S2CID 249050620. It is notable that the European Y-Hg I2a1a2b1a1a was also specific for the Conqueror group, especially for the elite as also shown before,34 very often accompanied by Asian maternal lineages, indicating that I2a1a2b1a1a could be more typical for the immigrants than to the local population.
  34. ^ Pamjav H, Fehér T, Németh E, Koppány Csáji L (2019). Genetika és őstörténet (in Hungarian). Napkút Kiadó. p. 58. ISBN 978-963-263-855-3. Az I2-CTS10228 (köznevén „dinári-kárpáti") alcsoport legkorábbi közös őse 2200 évvel ezelőttre tehető, így esetében nem arról van szó, hogy a mezolit népesség Kelet-Európában ilyen mértékben fennmaradt volna, hanem arról, hogy egy, a mezolit csoportoktól származó szűk család az európai vaskorban sikeresen integrálódott egy olyan társadalomba, amely hamarosan erőteljes demográfiai expanzióba kezdett. Ez is mutatja, hogy nem feltétlenül népek, mintsem családok sikerével, nemzetségek elterjedésével is számolnunk kell, és ezt a jelenlegi etnikai identitással összefüggésbe hozni lehetetlen. A csoport elterjedése alapján valószínűsíthető, hogy a szláv népek migrációjában vett részt, így válva az R1a-t követően a második legdominánsabb csoporttá a mai Kelet-Európában. Nyugat-Európából viszont teljes mértékben hiányzik, kivéve a kora középkorban szláv nyelvet beszélő keletnémet területeket.
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  38. ^ "I-M223 YTree".
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  40. ^ YFull, 2021, I-M284
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External links

  • YFull YTree of I2
  • FTDNA Y-DNA Haplotree of I
  • ISOGG 2019-2020 Y-DNA Haplogroup I and its Subclades

Relationship to haplogroups and subclades

haplogroup, m438, this, article, needs, attention, from, expert, human, genetic, history, specific, problem, nomenclature, haplogroup, subclades, wikiproject, human, genetic, history, able, help, recruit, expert, november, 2015, also, known, isogg, 2019, human. This article needs attention from an expert in Human Genetic History The specific problem is Nomenclature of haplogroup s and subclades WikiProject Human Genetic History may be able to help recruit an expert November 2015 Haplogroup I M438 also known as I2 ISOGG 2019 is a human DNA Y chromosome haplogroup a subclade of Haplogroup I M170 Haplogroup I M438 originated some time around 26 000 31 000 BCE It originated in Europe and developed into several main subgroups I2 M438 I2a L460 I2b L415 and I2c L596 2 The haplogroup can be found all over Europe and reaches its maximum frequency in the Dinaric Alps Balkans via founder effect 4 Examples of basal I M438 have been found in males from Crete and Sicily 5 Haplogroup I M438Possible time of origin28 33 000 years ago 1 Possible place of originSouth Eastern or Eastern Europe AncestorI M170DescendantsI L460 I L1251Defining mutationsM438 P215 S31Highest frequenciesI2a1a Sardinia 2 I2a1b Bosnia and Herzegovina 3 I2a2 Britain Germany and Sweden 2 Contents 1 Origin amp prehistoric presence 2 Subclades of I L460 2 1 I P37 2 2 1 1 I L158 2 1 2 I L178 2 1 2 1 I2a L621 2 2 I M223 2 2 1 I M284 2 2 2 I CTS10057 2 2 2 1 I Z161 2 2 2 2 I L701 2 3 I M436 3 Subclades list 4 See also 5 Notes 6 References 7 External links 8 Relationship to haplogroups and subcladesOrigin amp prehistoric presence EditThis section needs expansion You can help by adding to it April 2017 Haplogroup I2a was the most frequent Y DNA among western European mesolithic hunter gatherers WHG belonging to Villabruna Cluster A 2015 study found haplogroup I2a in 13 500 year old remains from the Azilian culture from Grotte du Bichon modern Switzerland 6 Subclades of I2a1 I P37 2 namely I M423 and I M26 have been found in remains of Western European Hunter Gatherers dating from 10 000 to 8 000 years before present respectively 7 In a 2015 study published in Nature the remains of six individuals from Motala ascribed to the Kongemose culture were successfully analyzed With regards to Y DNA two individuals were ascribed to haplogroup I2a1b one individual was ascribed to haplogroup I2a1 and one individual was ascribed to haplogroup I2c 8 Subclades of I L460 EditI P37 2 Edit The I P37 2 also known as I2a1a ISOGG 2019 The subclade divergence for I P37 2 occurred 10 7 4 8 kya The age of YSTR variation for the P37 2 subclade is 8 0 4 0 kya 2 It is the predominant version of I2 in Eastern Europe 9 The I2a is further made up by sub groups I M26 I M423 I L1286 I L880 I L158 Edit Haplogroup I M26 or M26 I2a1a1a ISOGG 2019 Haplogroup I L158 L158 L159 1 S169 1 M26 accounts for approximately 40 of all patrilines among the Sardinians 10 11 It is also found at low to moderate frequency among populations of the Pyrenees 9 5 in Bortzerriak Navarra 9 7 in Chazetania Aragon 8 in Val d Aran Catalunya 2 9 in Alt Urgell Catalunya and 8 1 in Baixa Cerdanya Catalunya and Iberia and it has been found in 1 6 of a sample of Albanians living in the Republic of North Macedonia 12 and 1 2 3 257 of a sample of Czechs 13 The age of YSTR variation for the M26 subclade has been calculated at 8 0 4 0 kya 2 I L178 Edit I L178 is very rare but has been found in two persons from Germany and one from Poland The age of YSTR variation for the M423 subclade is 8 8 3 6 kya 1 I2a L621 Edit The approximate frequency and variance distribution of haplogroup I P37 clusters ancestral Dnieper Carpathian DYS448 20 and derived Balkan DYS448 19 represented by a single SNP I PH908 in Eastern Europe per O M Utevska 2017 I2a1a2b L621 is typical of the Slavic populations being highest in Southeastern European regions of Bosnia Herzegovina and South Croatia gt 45 3 14 15 in Bosniaks 43 53 52 17 Croats 37 7 69 8 and Serbs 36 6 42 because of which is often called Dinaric 16 It has the highest variance and also high concentration in Eastern Europe Ukraine Southeastern Poland Belarus 17 According to YFull YTree it formed 11 400 YBP and had TMRCA 6 500 YBP while its main subclades lineage is I CTS10936 6 500 5 600 YBP gt I S19848 5 600 YBP gt I CTS4002 5 600 5 100 YBP gt I CTS10228 5 100 3 400 YBP gt I Y3120 3 400 2 100 YBP gt I Y18331 2 100 YBP I Z17855 2 100 1650 YBP I Y4460 2 100 YBP I S17250 2 100 1 850 YBP gt I PH908 1 850 1 700 YBP 18 Older research considered that the high frequency of this subclade in the South Slavic speaking populations to be the result of pre Slavic paleolithic settlement in the region Pericic et al 2005 for instance place its expansion to have occurred not earlier than the YD to Holocene transition and not later than the early Neolithic 2 3 19 20 However the prehistoric autochthonous origin of the haplogroup I2 in the Balkans is now considered as out of date nb 1 as already Battaglia et al 2009 observed highest variance of the haplogroup in Ukraine and Zupan et al 2013 noted that it suggests it arrived with Slavic migration from the homeland which was in present day Ukraine 25 The research by O M Utevska 2017 concluded that the haplogroup STR haplotypes have the highest diversity in Ukraine with ancestral STR marker result DYS448 20 comprising Dnieper Carpathian cluster while younger derived result DYS448 19 comprising the Balkan cluster which is predominant among the South Slavs 17 This Balkan cluster also has the highest variance in Ukraine which indicates that the very high frequency in the Western Balkan is because of a founder effect 17 Utevska calculated that the STR cluster divergence and its secondary expansion from the middle reaches of the Dnieper river or from Eastern Carpathians towards the Balkan peninsula happened approximately 2 860 730 years ago relating it to the times before Slavs but much after the decline of the Cucuteni Trypillia culture 17 However STR based calculations give overestimated dates 26 27 and more specifically the Balkan cluster is represented by a single SNP I PH908 known as I2a1a2b1a1a1c in ISOGG phylogenetic tree 2019 and according to YFull YTree it formed and had TMRCA approximately 1 850 1 700 YBP 2nd 3rd century AD 18 It is considered that I L621 could have been present in the Cucuteni Trypillia culture 28 but until now was mainly found G2a and non I2 L621 clades 29 30 and another clade I2a1a1 CTS595 was present in the Baden culture of the Chalcolithic Carpathian Basin 28 31 32 Although it is dominant among the modern Slavic peoples on the territory of the former Balkan provinces of the Roman Empire until now it was not found among the samples from the Roman period and is almost absent in contemporary population of Italy 16 It was found in the skeletal remains with artifacts indicating leaders of Hungarian conquerors of the Carpathian Basin from the 9th century part of Western Eurasian Slavic component of the Hungarians 16 28 33 According to Pamjav et al 2019 and Fothi et al 2020 the distribution of ancestral subclades like of I CTS10228 among contemporary carriers indicates a rapid expansion from Southeastern Poland is mainly related to the Slavs and their medieval migration and the largest demographic explosion occurred in the Balkans 16 34 The earliest archeogenetic sample until now is Sungir 6 900 YBP near Vladimir Russia which belonged to the I S17250 gt I Y5596 gt I Z16971 gt I Y5595 gt I A16681 subclade 35 36 as well I CTS10228 and I Y3120 subclades were found in two Viking samples from Sweden VK53 and Ukraine VK542 with predominantly Slavic ancestry of which the second belongs to Gleb Svyatoslavich 11th century 37 I M223 Edit Haplogroup I M223 aka I2a1b1 ISOGG 2019 formerly I2a2a ISOGG 2014 The age of YSTR variation for the I M223 subclade has been variously estimated as 13 2 2 7 kya 2 12 3 3 1 kya 1 14 6 kya 38 and 14 6 3 8 kya Rootsi 2004 I M223 has a peak in Germany and another in the northeast of Sweden but also appears in Romania Moldova Russia Greece Italy and around the Black Sea 39 Haplogroup I M223 has been found in over 4 of the population only in Germany the Netherlands Belgium Denmark Scotland and England excluding Cornwall also the southern tips of Sweden and Norway in Northwest Europe the provinces of Normandy Maine Anjou and Perche in northwestern France the province of Provence in southeastern France the regions of Tuscany Umbria and Latium in Italy Moldavia and the area around Russia s Ryazan Oblast and Mordovia in Eastern Europe Of historical note both haplogroups I M253 and I M223 appear at a low frequency in the historical regions of Bithynia and Galatia in Turkey Haplogroup I M223 also occurs among approximately 1 of Sardinians I M284 Edit Haplogroup I2a1b1a1a ISOGG 2019 or I M284 has been found almost exclusively amongst the populations of the United Kingdom and Ireland suggesting that it may have arisen amongst the Ancient Britons with a most recent common ancestor MRCA who lived about 3 100 years BP 40 The presence of this subclade provides some tentative evidence of ancient flow with eastern areas that could support the idea that the late Celtic La Tene culture was accompanied by some migration 41 Where it is found in those of predominately Irish descent with Gaelic surnames it may suggest an ancestor who arrived in Ireland during prehistory from Celtic Britain 41 For example I M284 includes many males with the surnames McGuinness and McCartan who have a single historically recorded male ancestor in the 6th century thus it is unlikely to be the result of subsequent migration from Britain to Ireland 41 Some subclades of I M284 that are atypical of Ireland are relatively common in continental Europe 41 which also supports a point of origin east of Ireland I CTS10057 Edit Continentals Mother Haplogroup for group I Z161 Continental 1 and 2 and I L701 group Continental 3 Around 10 000 years old I Z161 Edit Haplogroup I2a1b1a2b ISOGG 2019 Z161 defines the I2 Continental clade 1 and 2 Its age is estimated around 7 000 years old It is mainly found in North Europe especially in Denmark Germany the Netherlands and England In Northwest Sicily it can also be found this is believed to be due to remnants of a Norman settlement I L701 Edit Called Continental 3 Continental 3 has a wide distribution Found in Central Europe from Germany Austria to Poland Romania and Ukraine but also in lower frequencies in Greece Italy France Spain England Ireland and Armenia It may have been disseminated in part by the Goths It is nearly absent from Scandinavia and Scotland I M436 Edit This section needs expansion You can help by adding to it January 2021 Subclades list EditThis section does not cite any sources Please help improve this section by adding citations to reliable sources Unsourced material may be challenged and removed November 2015 Learn how and when to remove this template message Up to date phylogenetic trees listing subclades of I can be found at Y Full and FamilyTreeDNA Haplogroup I I1 I1aI1bI1cI1dI1eI2 I2aI2bI2 Subclades list I2 M438 P215 PF3853 S31 16638804 A gt G I2a L460 PF3647 S238 7879415 A gt C I2a1 P37 2 PF4004 14491684 T gt C I2a1a CTS595 6874115 C gt T I2a1a1 M26 PF4056 21865821 G gt A I2a1a1a CTS8968 PF4036 18584762 T gt C I2a1a1a1 L672 S327 22228628 T gt A I2a1a1a1a L160 PF4013 S184 I2a1a1a2 CTS6027 16620529 C gt G w Europeans I2a1a1a3 Z27395 16681589 A gt G I2a1a1a3a Z27410 18891640 T gt G I2a1a1a3a1 Z27430 15383072 T gt C I2a1a1a3a1a Z27446 14420039 G gt A I2a1a1a3a1a1 Z27447 17445510 A gt G I2a1a1a3a1a1a Z27452 7346620 C gt T Sardinians I2a1a1a3a1a1b Z27453 22045753 C gt A I2a1a1a3a1a1b1 Z27456 13885862 T gt C Sardinians I2a1a1b Z27354 7132292 T gt C I2a1a1b1 Z27400 2833818 C gt T Sardinians I2a1a2 S21825 19126655 G gt A I2a1a2a L1286 21778662 G gt A I2a1a2a1 L1287 21970862 G gt T I2a1a2a1a L233 S183 14487362 G gt A I2a1a2a1a1 A417 8846964 T gt C Brits I2a1a2a2 L880 3436270 C gt T central Europeans I2a1a2b L1294 2887401 T gt C French I2a1a3 S2699 14434372 C gt T I2a1b M423 19096091 G gt A I2a1b1 L161 1 S185 1 22513718 C gt T I2a1b1a L1498 Y4008 18668472 C gt T I2a1b1a1 FGC7218 Y5280 21354226 G gt A Irish I2a1b1a2 FGC14448 Y5450 7158983 A gt G Irish I2a1b1a3 FGC7108 S2640 14107847 G gt A I2a1b1a3a FGC7197 S7703 17494645 G gt C I2a1b1a3a1 S7714 21345894 T gt A I2a1b1a3a1a S8889 4310132 A gt G I2a1b1a3b S2742 19440521 A gt G I2a1b1a3c FGC7173 Y3729 8472670 A gt T I2a1b1a3c1 FGC7156 Y4665 2685333 T gt C I2a1b1a3c1a FGC7218 Y5280 21354226 G gt A I2a1b1a3c2 FGC14453 Y5456 16637771 A gt G I2a1b1a4 A1150 15543414 A gt T I2a1b1b PF4135 18981938 G gt A Brits I2a1b1c CTS8849 2 18236845 A gt G I2a1b1d PF6316 2 18181850 T gt G I2a1b2 L621 S392 18760081 G gt A I2a1b2a CTS4002 15328797 C gt A I2a1b2a1 CTS10228 9334357 A gt C I2a1b2a1a S17250 YP204 15531354 G gt A I2a1b2a1a1 Z16971 6676628 G gt C Slovenians Germans Ukrainians I2a1b2a1a2 Y3548 14856842 A gt G Sardinians I2a1b2a1a2a Y4882 21135222 G gt A Poles I2a1b2a1a3 A356 Z16983 17558968 T gt C I2a1b2a1a3a Y6651 23792119 A gt G Czechs I2a1b2a1b Y4460 9028830 G gt A I2a1b2a1b1 Y3118 23548545 T gt C I2a1b2a1b1a CTS5579 S5054 16378157 G gt T Finns I2a1b2a1b V19 2 2189 200 T gt C I2a1b2a1c P61 2 14482194 G gt A I2a2 M436 P214 PF3856 S33 18747493 G gt C I2a2a M223 21717307 G gt A I2a2a1 CTS616 6906332 G gt C I2a2a1a Y3721 7982615 C gt T I2a2a1a1 M284 22750461 22750464 ACAA gt del I2a2a1a1a L1195 18865320 G gt A I2a2a1a1a1 L126 S165 14901633 C gt T I2a2a1a1a1a FGC20048 S7753 Y4171 17603051 G gt T I2a2a1a1a1a1 FGC20065 Y4751 18635722 A gt G I2a2a1a1a1a1a Y4750 23059262 C gt G I2a2a1a1a1a1a1 FGC20062 Y4753 16910733 G gt T Irish Scots I2a2a1a1a1a1a2 Y8599 Irish I2a2a1a1a1b Y7190 7987909 C gt T Scots I2a2a1a1a1c F3878 2 8752246 G gt A I2a2a1a1a2 L1193 9448484 C gt A I2a2a1a1a2a CTS4922 15903939 T gt C I2a2a1a1a2a1 FGC14237 Y5996 8292320 G gt T Irish I2a2a1a1a2b CTS3792 S2380 15183633 C gt T I2a2a1a2 Z2057 4770006 T gt C I2a2a1a2a L1229 14937828 C gt A I2a2a1a2a1 Y3681 22519059 T gt C I2a2a1a2a1a Z2058 5317533 T gt C I2a2a1a2a1a1 Z2054 2980725 C gt T I2a2a1a2a1a1a BY524 Y9443 6371561 A gt G I2a2a1a2a1a1a1 L812 S391 14850035 G gt A I2a2a1a2a1a1a1a Y5308 16820196 G gt A I2a2a1a2a1a1a2 Y10648 8267867 C gt G I2a2a1a2a1a1b Y7244 8271590 C gt T Germans I2a2a1a2a1a1b1 P53 3 14491649 T gt C I2a2a1a2a1a1b2 Y7243 2911078 G gt A I2a2a1a2a1a1c FGC15106 Y4334 7845669 G gt T I2a2a1a2a1a1c1 FGC15128 Y4714 15945966 G gt C Irish I2a2a1a2a1a1c2 Y4760 15025945 A gt T Brits Germans I2a2a1a2a1a1d BY138 2809424 A gt T Mexicans English I2a2a1a2a2 S18331 16449714 C gt T Brits I2a2a1a2a2a L1230 3436442 G gt A Brits I2a2a1a2b Y7240 2688254 T gt G English I2a2a1b CTS10057 19232160 C gt T I2a2a1b1 L702 7629205 C gt T I2a2a1b1a P78 6740387 G gt A I2a2a1b1a1 S25733 23595728 C gt T I2a2a1b1a1a A427 23281929 G gt T I2a2a1b1a1a1 S23612 21826246 C gt T Brits Italians Germans I2a2a1b1a1a1a Y5360 23185624 G gt T I2a2a1b1a1a1b S10702 7822881 T gt C I2a2a1b1a1a2 Y5369 23185624 G gt T Brits I2a2a1b1a2 Y7219 8447173 C gt A I2a2a1b1a2a Y7214 4901002 C gt A Dutch I2a2a1b1a2b Y8945 4567154 G gt A I2a2a1b1b L699 2663920 A gt G I2a2a1b1b1 L704 17595966 C gt A I2a2a1b1b1a S12195 9105096 C gt T I2a2a1b1b1a1 Y6973 8430276 A gt G I2a2a1b1b2 Z26416 18851267 G gt A Sardinians I2a2a1b1b3 PF6901 17558585 C gt G Sardinians I2a2a1b1c PF6896 8904322 C gt T Brits French I2a2a1b2 Z161 2696497 C gt G I2a2a1b2a L801 S390 21763755 A gt C I2a2a1b2a1 CTS1977 14140273 G gt A I2a2a1b2a1a Y5282 7982615 C gt T I2a2a1b2a1a1 S8522 3162610 T gt C I2a2a1b2a1a1a P95 14869706 G gt T Poles n w Europeans I2a2a1b2a1a2 CTS1858 14098206 G gt T I2a2a1b2a1a2a CTS10148 19291083 A gt T African Americans I2a2a1b2a1b Y7152 5852771 C gt T I2a2a1b2a1c BY526 or Y8935 I2a2a1b2a2 CTS6433 16889964 T gt C I2a2a1b2a2a S2364 23052606 A gt G I2a2a1b2a2a1 FGC3618 S2361 17355245 A gt G I2a2a1b2a2a1a Z78 9154908 T gt C I2a2a1b2a2a1a1 CTS8584 I2a2a1b2a2a1a1a Z185 22929384 T gt C I2a2a1b2a1b1a1a1 Z180 22065434 A gt G I2a2a1b2a1b1a1a1a L1198 18405788 C gt T I2a2a1b2a1b1a1a1a1 Z190 17473966 G gt T I2a2a1b2a1b1a1a1a1a S434 Z79 17147721 G gt A English I2a2a1b2a1b1a1a1a1a1 Y5729 14394460 C gt T English I2a2a1b2a1b1a1a1a1a2 Y7682 not yet reported I2a2a1b2a1b1a1a1a1b Y7280 17305030 T gt G I2a2a1b2a1b1a1a1a2 FGC3617 S2368 Z166 14010863 G gt T I2a2a1b2a1b1a1a1a3 P195 2 22665262 A gt G Brits I2a2a1b2a1b1a1a1b Y5748 14106278 C gt T I2a2a1b2a1b1a1a1b1 Y7272 19264274 G gt A I2a2a1b2a1b1a1a1c Y7273 16449864 A gt G I2a2a1b2a1b1a2 Y9161 9154908 T gt C I2a2a1b2a1b1b Y4925 ZS20 23977120 A gt C I2a2a1b2a1b1b1 CTS661 L1272 6931960 G gt A I2a2a1b2a1b1b1a Y5717 6931960 G gt A I2a2a1b2a1b1b2 FGC17399 Y4926 23549293 G gt A I2a2a1b2a1b1b2a S8104 7432604 A gt G I2a2a1b2a1b1c Y4955 15362162 G gt A I2a2a1b2a1b1c1 Y5695 14574229 T gt C I2a2a1b2a1b1c1a Y7263 7900806 C gt A I2a2a1b2a1b1c1a1 Y7265 9147689 T gt C I2a2a1b2a1b1c1b FGC20004 Y5692 18993826 A gt T I2a2a1b2a1b1c2 Y10659 4616653 A gt G I2a2a1b2a1b2 L1425 14491835 C gt T I2a2a1b2a1b2a CTS5332 2 PF7472 2 16212441 G gt A I2a2a1b2a1b2b Y4769 18201094 A gt G Germans I2a2a1b2a1b3 Y7426 18830768 A gt G English I2a2a1b2a1b4 S243 Z63 14401486 C gt T I2a2a1b2a1b5 M3268 2 PF3292 2 8519704 G gt A Germans I2a2a1b2a1b6 DF5 2 S191 2 18393814 A gt G Brits I2a2a1b2a1b7 F3406 2 23119516 G gt A I2a2a1b2a2 L1290 14623983 T gt C n Europeans I2a2a1b2a3 Y7202 2913976 G gt A Germans I2a2a1b2b L623 16202490 A gt T I2a2a1b2c CTS11871 S3673 23326304 C gt T Brits Germans I2a2a1b2d Y5188 7838639 G gt A Maltese I2a2a1b3 S12606 9879942 T gt G I2a2a1b3a CTS12640 S4904 ZS21 28652639 C gt T I2a2a2 S9403 SK1254 6742730 T gt C I2a2a2a L1228 15446045 G gt C w Europeans I2a2a2b Y6099 7527993 G gt A I2a2b L38 S154 15668070 A gt G I2a2b1 L533 S295 2887198 G gt C n w Europeans I2a2b2 S2606 22527402 C gt A I2a2b2a S2523 14951410 C gt T I2a2b2a1 S24121 22201497 C gt A I2a2b2a1a S11558 8491250 G gt A I2a2b2a1b F780 2 6384078 G gt A I2a2b3 M8990 S3846 7534645 A gt C I2a2b3a S2488 12733783 T gt A English I2a2b3b S4556 14124389 A gt G I2a2b4 P15 2 PF3112 2 3244026 C gt T I2b L415 S435 2888663 C gt T or L417 S332 8426321 T gt C Germans Italians I2c L596 PF6907 S292 14197631 G gt A or L597 S333 18887888 T gt A I2c1 PF3892 8487200 T gt C I2c1a L1251 2888598 C gt T Germans I2c1b CTS4092 15391894 G gt A I2c1b1 CTS7767 1 17651573 C gt A I2c1b1a PF6328 21797244 C gt A I2c1b1a1 F2044 15944600 T gt A Brits I2c1c S6685 14185048 G gt C I2c1c1 S6648 14459289 T gt A I2c1c1a FGC18548 7380574 A gt G Sardinians I2c1c1b S6716 16173282 G gt C I2c1c1b1 S6622 14264992 A gt G I2c1c1b1a S6595 21430083 G gt A I2c1c1b1a1 S6656 17410728 G gt C I2c1c1c S9234 6512608 A gt G I2c2 PF3827 22444389 T gt A I2c3 S6800 16180130 G gt A See also EditHuman Y chromosome DNA haplogroups Haplogroup I Y DNA Haplogroup I1 Y DNA Notes Edit The SNP I P37 itself formed approximately 21 000 YBP and had TMRCA 18 400 YBP according to YFull YTree 21 being too old and widespread as an SNP for argumentation of ancient autochthony or medieval migration as well the old research used outdated nomenclature According to I P37 I2a project at Family Tree DNA the divergence at STR marker DYS448 20 gt 19 is reported since 2007 22 while the SNP which defines the STR Dinaric South cluster I PH908 is reported since 2014 23 The SNP I PH908 at ISOGG phylogenetic tree is named as I2a1a2b1a1a1c 24 while formed and had TMRCA approximately 1 800 YBP according to YFull 18 References Edit a b c Underhill PA Myres NM Rootsi S Chow CT Lin AA Otillar RP et al 2007 New phylogenetic relationships for Y chromosome haplogroup I Reappraising its Phylogeography and Prehistory In Mellars P Boyle K Bar Yosef O Stringer C eds Rethinking the Human Evolution pp 33 42 ISBN 978 1 902937 46 5 a b c d e f g Rootsi S Magri C Kivisild T Benuzzi G Help H Bermisheva M et al July 2004 Phylogeography of Y chromosome haplogroup I reveals distinct domains of prehistoric gene flow in europe American Journal of Human Genetics 75 1 128 137 doi 10 1086 422196 PMC 1181996 PMID 15162323 a b c Pericic M Lauc LB Klaric IM Rootsi S Janicijevic B Rudan I et al October 2005 High resolution phylogenetic analysis of southeastern Europe traces major episodes of paternal gene flow among Slavic populations Molecular Biology and Evolution 22 10 1964 1975 doi 10 1093 molbev msi185 PMID 15944443 Grasgruber P Popovic S Bokuvka D Davidovic I Hrebickova S Ingrova P et al April 2017 The mountains of giants an anthropometric survey of male youths in Bosnia and Herzegovina Royal Society Open Science 4 4 161054 Bibcode 2017RSOS 461054G doi 10 1098 rsos 161054 PMC 5414258 PMID 28484621 What are Haplogroups Living DNA explain Living DNA 2020 03 19 Archived from the original on 2022 08 20 Retrieved 2022 08 20 Jones ER Gonzalez Fortes G Connell S Siska V Eriksson A Martiniano R et al November 2015 Upper Palaeolithic genomes reveal deep roots of modern Eurasians Nature Communications 6 8912 Bibcode 2015NatCo 6 8912J doi 10 1038 ncomms9912 PMC 4660371 PMID 26567969 1 Archived 2017 04 30 at the Wayback Machine Mesolithic Western Eurasian DNA Mathieson I Lazaridis I Rohland N Mallick S Patterson N Roodenberg SA et al December 2015 Genome wide patterns of selection in 230 ancient Eurasians Nature 528 7583 499 503 Bibcode 2015Natur 528 499M doi 10 1038 nature16152 PMC 4918750 PMID 26595274 Sazzini M Sarno S Luiselli D 2014 The Mediterranean Human Population An Anthropological Genetics Perspective The Mediterranean Sea pp 529 551 doi 10 1007 978 94 007 6704 1 31 ISBN 978 94 007 6703 4 Rootsi S 31 December 2006 Y Chromosome haplogroup I prehistoric gene flow in Europe Documenta Praehistorica 33 17 20 doi 10 4312 dp 33 3 Francalacci P Morelli L Angius A Berutti R Reinier F Atzeni R et al August 2013 Low pass DNA sequencing of 1200 Sardinians reconstructs European Y chromosome phylogeny Science 341 6145 565 569 Bibcode 2013Sci 341 565F doi 10 1126 science 1237947 PMC 5500864 PMID 23908240 Battaglia V Fornarino S Al Zahery N Olivieri A Pala M Myres NM et al June 2009 Y chromosomal evidence of the cultural diffusion of agriculture in Southeast Europe European Journal of Human Genetics 17 6 820 830 doi 10 1038 ejhg 2008 249 PMC 2947100 PMID 19107149 Luca F Di Giacomo F Benincasa T Popa LO Banyko J Kracmarova A et al January 2007 Y chromosomal variation in the Czech Republic American Journal of Physical Anthropology 132 1 132 139 doi 10 1002 ajpa 20500 hdl 2108 35058 PMID 17078035 Mrsic G Grskovic B Vrdoljak A Popovic M Valpotic I Anđelinovic S et al July 2012 Croatian national reference Y STR haplotype database Molecular Biology Reports 39 7 7727 7741 doi 10 1007 s11033 012 1610 3 PMID 22391654 S2CID 18011987 Kovacevic L Tambets K Ilumae AM Kushniarevich A Yunusbayev B Solnik A et al 2014 Standing at the gateway to Europe the genetic structure of Western balkan populations based on autosomal and haploid markers PLOS ONE 9 8 e105090 Bibcode 2014PLoSO 9j5090K doi 10 1371 journal pone 0105090 PMC 4141785 PMID 25148043 a b c d Fothi E Gonzalez A Feher T Gugora A Fothi A Biro O Keyser C 2020 Genetic analysis of male Hungarian Conquerors European and Asian paternal lineages of the conquering Hungarian tribes Archaeological and Anthropological Sciences 12 1 doi 10 1007 s12520 019 00996 0 We looked at 16 loci from 640 I2a L621 samples in FTDNA s I2a project database and found that 7 individuals were 2 genetic steps away the Karos samples of whom 1 was a Hungarian from Kunszentmarton 2 were Ukrainians 1 was Lithuanian 1 was Belarusian 1 was Russian and 1 was a German from Poland Based on SNP analysis the CTS10228 group is 2200 300 years old The group s demographic expansion may have begun in Southeast Poland around that time as carriers of the oldest subgroup are found there today The group cannot solely be tied to the Slavs because the proto Slavic period was later around 300 500 CE The SNP based age of the Eastern European CTS10228 branch is 2200 300 years old The carriers of the most ancient subgroup live in Southeast Poland and it is likely that the rapid demographic expansion which brought the marker to other regions in Europe began there The largest demographic explosion occurred in the Balkans where the subgroup is dominant in 50 5 of Croatians 30 1 of Serbs 31 4 of Montenegrins and in about 20 of Albanians and Greeks As a result this subgroup is often called Dinaric It is interesting that while it is dominant among modern Balkan peoples this subgroup has not been present yet during the Roman period as it is almost absent in Italy as well see Online Resource 5 ESM 5 Their genetic haplogroup I2a CTS10228 is widespread among Slavs but it is only present in 7 of Caucasian peoples namely among the Karachay As such it appears that the I2a CTS10228 haplogroup in the paternal lineage of the Karos leaders arises from a specific branch in the Northern Caucasus dating to about 400 500 CE Its modern descendents live among the Karachay Hungarians and various other surrounding nationalities a b c d O M Utevska 2017 Genofond ukrayinciv za riznimi sistemami genetichnih markeriv pohodzhennya i misce na yevropejskomu genetichnomu prostori The gene pool of Ukrainians revealed by different systems of genetic markers the origin and statement in Europe PhD in Ukrainian National Research Center for Radiation Medicine of National Academy of Sciences of Ukraine pp 219 226 302 a b c I PH908 YTree v8 06 01 YFull com 27 June 2020 Retrieved 17 July 2020 Marjanovic D Fornarino S Montagna S Primorac D Hadziselimovic R Vidovic S et al November 2005 The peopling of modern Bosnia Herzegovina Y chromosome haplogroups in the three main ethnic groups Annals of Human Genetics 69 Pt 6 757 763 doi 10 1111 j 1529 8817 2005 00190 x PMID 16266413 S2CID 36632274 Rebala K Mikulich AI Tsybovsky IS Sivakova D Dzupinkova Z Szczerkowska Dobosz A Szczerkowska Z 16 March 2007 Y STR variation among Slavs evidence for the Slavic homeland in the middle Dnieper basin Journal of Human Genetics 52 5 406 414 doi 10 1007 s10038 007 0125 6 PMID 17364156 I P37 YTree v8 06 01 YFull com 27 June 2020 Retrieved 17 July 2020 I2a Y Haplogroup Results I2a2a Dinaric Family Tree DNA Retrieved 11 November 2018 Ken Nordtvedt has split I2a2 M423 Dinaric into Din N and Din S Din N is older than Din S N north of the Danube and S south of the Danube River May 8 2007 Dinaric I1b1 and DYS 448 DYS448 19 for S and 20 for N Bernie Cullen 22 August 2016 Link to I L621 tree showing major STR clusters Updated i2aproject blogspot com Blogger Retrieved 3 April 2019 Y DNA Haplogroup I and its Subclades 2019 2020 ISOGG 1 October 2019 Retrieved 17 July 2020 Zupan A Vrabec K Glavac D 2013 The paternal perspective of the Slovenian population and its relationship with other populations Annals of Human Biology 40 6 515 526 doi 10 3109 03014460 2013 813584 PMID 23879710 S2CID 34621779 Sarac J Saric T Havas Augustin D Novokmet N Vekaric N Mustac M et al November 2016 Genetic heritage of Croatians in the Southeastern European gene pool Y chromosome analysis of the Croatian continental and Island population American Journal of Human Biology 28 6 837 845 doi 10 1002 ajhb 22876 PMID 27279290 S2CID 25873634 It is important to stress that the proposed old age of the I2a1b M423 and R1a1a1b1a M558 lineages obtained in previous studies Battaglia et al 2009 Pericic et al 2005 Rootsi et al 2004 Underhill et al 2007 2015 has been based on STR analysis 8 and 10 loci respectively and recent studies clearly indicate that the STR based age calculations tend to yield overestimated dates Batini et al 2015 Hallast et al 2015 Karmin et al 2015 Balanovsky O May 2017 Toward a consensus on SNP and STR mutation rates on the human Y chromosome Human Genetics 136 5 575 590 doi 10 1007 s00439 017 1805 8 PMID 28455625 S2CID 3714493 While the reasons for the difference between genealogical and evolutionary Y STR rates are thus partly understood it remains unclear which rate to use Many have applied the evolutionary rate though quite a few have used the genealogical or both rates Genetic genealogists generally apply the genealogical rate and criticize population genetic studies for reporting in their view three times overestimated ages The age of each haplogroup was also calculated using the STR genealogical rate and the STR evolutionary rate Confidence intervals for the two STR based ages not shown on the plot do not overlap For example the genealogical age of I2a L621 2200 500 years reaches the envelope age from 2600 to 3100 ages while the evolutionary age lies far beyond 9900 2700 years The observed pattern Fig 2a clearly differs for haplogroups of different age classes For ages less than 7000 years the genealogical STR rate provides results consistent with or slightly underestimating the true ages while the evolutionary rate results in three fold overestimates For ages between roughly 7000 and 15 000 years neither STR rate provides correct results For haplogroups older than 15 000 years the evolutionary rate estimates correctly or overestimates the true age a b c Neparaczki E Maroti Z Kalmar T Maar K Nagy I Latinovics D et al November 2019 Y chromosome haplogroups from Hun Avar and conquering Hungarian period nomadic people of the Carpathian Basin Scientific Reports Nature Research 9 1 16569 Bibcode 2019NatSR 916569N doi 10 1038 s41598 019 53105 5 PMC 6851379 PMID 31719606 Hg I2a1a2b L621 was present in 5 Conqueror samples and a 6th sample form Magyarhomorog MH 9 most likely also belongs here as MH 9 is a likely kin of MH 16 see below This Hg of European origin is most prominent in the Balkans and Eastern Europe especially among Slavic speaking groups It might have been a major lineage of the Cucuteni Trypillian culture and it was present in the Baden culture of the Calcholitic Carpathian Basin24 The identical I2a1a2b Hg s of Magyarhomorog individuals appears to be frequent among high ranking Conquerors as the most distinguished graves in the Karos2 and 3 cemeteries also belong to this lineage Mathieson I Alpaslan Roodenberg S Posth C Szecsenyi Nagy A Rohland N Mallick S et al March 2018 The genomic history of southeastern Europe Nature 555 7695 197 203 Bibcode 2018Natur 555 197M doi 10 1038 nature25778 PMC 6091220 PMID 29466330 Gelabert P Schmidt RW Fernandes DM Karsten JK Harper TK Madden GD et al May 2022 Genomes from Verteba cave suggest diversity within the Trypillians in Ukraine Scientific Reports Nature Research 12 1 7242 doi 10 1038 s41598 022 11117 8 PMC 9068698 PMID 35508651 Lipson M Szecsenyi Nagy A Mallick S Posa A Stegmar B Keerl V et al November 2017 Parallel palaeogenomic transects reveal complex genetic history of early European farmers Nature 551 7680 368 372 Bibcode 2017Natur 551 368L doi 10 1038 nature24476 PMC 5973800 PMID 29144465 Patterson N Isakov M Booth T Buster L Fischer CE Olalde I et al January 2022 Large scale migration into Britain during the Middle to Late Bronze Age Nature 601 7894 588 594 Bibcode 2022Natur 601 588P doi 10 1038 s41586 021 04287 4 PMC 8889665 PMID 34937049 S2CID 245509501 Maroti Z Neparaczki E Schutz O Maar K Varga GI Kovacs B et al July 2022 The genetic origin of Huns Avars and conquering Hungarians Current Biology 32 13 2858 2870 e7 doi 10 1016 j cub 2022 04 093 PMID 35617951 S2CID 249050620 It is notable that the European Y Hg I2a1a2b1a1a was also specific for the Conqueror group especially for the elite as also shown before 34 very often accompanied by Asian maternal lineages indicating that I2a1a2b1a1a could be more typical for the immigrants than to the local population Pamjav H Feher T Nemeth E Koppany Csaji L 2019 Genetika es ostortenet in Hungarian Napkut Kiado p 58 ISBN 978 963 263 855 3 Az I2 CTS10228 kozneven dinari karpati alcsoport legkorabbi kozos ose 2200 evvel ezelottre teheto igy eseteben nem arrol van szo hogy a mezolit nepesseg Kelet Europaban ilyen mertekben fennmaradt volna hanem arrol hogy egy a mezolit csoportoktol szarmazo szuk csalad az europai vaskorban sikeresen integralodott egy olyan tarsadalomba amely hamarosan eroteljes demografiai expanzioba kezdett Ez is mutatja hogy nem feltetlenul nepek mintsem csaladok sikerevel nemzetsegek elterjedesevel is szamolnunk kell es ezt a jelenlegi etnikai identitassal osszefuggesbe hozni lehetetlen A csoport elterjedese alapjan valoszinusitheto hogy a szlav nepek migraciojaban vett reszt igy valva az R1a t kovetoen a masodik legdominansabb csoportta a mai Kelet Europaban Nyugat Europabol viszont teljes mertekben hianyzik kiveve a kora kozepkorban szlav nyelvet beszelo keletnemet teruleteket Sikora M Seguin Orlando A Sousa VC Albrechtsen A Korneliussen T Ko A et al November 2017 Ancient genomes show social and reproductive behavior of early Upper Paleolithic foragers Science 358 6363 659 662 Bibcode 2017Sci 358 659S doi 10 1126 science aao1807 PMID 28982795 I A16681 YTree v8 06 01 YFull com 27 June 2020 Retrieved 17 July 2020 Margaryan A Lawson DJ Sikora M Racimo F Rasmussen S Moltke I et al September 2020 Population genomics of the Viking world Nature 585 7825 390 396 Bibcode 2020Natur 585 390M bioRxiv 10 1101 703405 doi 10 1038 s41586 020 2688 8 hdl 10852 83989 PMID 32939067 S2CID 221769227 I M223 YTree Chiaroni J Underhill PA Cavalli Sforza LL December 2009 Y chromosome diversity human expansion drift and cultural evolution Proceedings of the National Academy of Sciences of the United States of America 106 48 20174 20179 Bibcode 2009PNAS 10620174C doi 10 1073 pnas 0910803106 PMC 2787129 PMID 19920170 YFull 2021 I M284 a b c d McEvoy BP Bradly DG 2010 Irish Genetics and Celts In Cunliffe BW Koch JT eds Celtic from the West Alternative Perspectives from Archaeology Genetics Language and Literature Oxbow Books pp 107 120 ISBN 978 1 84217 410 4 External links EditYFull YTree of I2 FTDNA Y DNA Haplotree of I ISOGG 2019 2020 Y DNA Haplogroup I and its SubcladesRelationship to haplogroups and subclades Edit Retrieved from https en wikipedia org w index php title Haplogroup I M438 amp oldid 1131114836, wikipedia, wiki, book, books, library,

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