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Haplogroup HV derives from the haplogroup R0, which in turn descends from haplogroup R.HV is also the ancestral clade to the haplogroups H and V.A possible origin of HV haplogroup is in the region of Western Iran, Mesopotamia, and the South Caucasus, where the highest prevalence of HV has been found.
Macro-haplogroup L is the most basal of human mtDNA haplogroups, from which all other haplogroups descend (specifically, from haplogroup L3). It is found mostly in Africa. Haplogroup L0; L1-7 Haplogroup L1; L2-7 L3'4'6 Haplogroup L2
Haplogroup HV derives from the haplogroup R0 which in turn derives from haplogroup R is a descendant of macro-haplogroup N like its sibling M, is a descendant of haplogroup L3. MtDNA H had frequency of 19% among Neolithic Early European Farmers and virtually absent among Mesolithic European hunter gatherers. [6]
Haplogroup R0 derives from the macro-haplogroup R. It is an ancestral clade to the R0a subclade and haplogroup HV , and is therefore antecedent to the haplogroups H and V . R0's greater subclade variety in the Arabian Peninsula suggests that the clade originated in and spread from there.
Haplogroups can be used to define genetic populations and are often geographically oriented. For example, the following are common divisions for mtDNA haplogroups: African: L0, L1, L2, L3, L4, L5, L6; West Eurasian: H, T, U, V, X, K, I, J, W (all listed West Eurasian haplogroups are derived from macro-haplogroup N) [10]
HV: JT: K: H: V: J: T: Pages in category "Human mtDNA haplogroups" The following 55 pages are in this category, out of 55 total. This list may not reflect recent ...
More than 90% of European mtDNAs belong to nine haplogroups (Fig. 1), which are highly specific for Western Eurasia (4, 6). These clusters are all thought to originate from one supercluster, L3n (N). The main determinants of this PC analysis are therefore the HV supercluster members, haplogroups H, HV, and pre-HV. Actually, whereas in the ...
Getting HVR1 and HVR2 DNA tests can help determine one's haplogroup. In the revised Cambridge Reference Sequence of the human mitogenome, the most variable sites of HVR1 are numbered 16024-16383 (this subsequence is called HVR-I), and the most variable sites of HVR2 are numbered 57-372 ( i.e., HVR-II) and 438-574 ( i.e., HVR-III).