Human (GRCh37.p13)

Assembly exceptions

GRC assembly patches, haplotype (HAPs) and pseudo autosomal regions (PARs)

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Assembly exceptions

GRC assembly patches, haplotype (HAPs) and pseudo autosomal regions (PARs)

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24 mapped markers found:

A004N12chromosome 8:10622711-10622970
A005E28chromosome 8:10286245-10286390
D8S1492chromosome 8:10620935-10621062
D8S453chromosome 8:10644518-10644781
D8S520chromosome 8:10556362-1055655410556377-10556559
G31054chromosome 8:10244165-10244300
G42365chromosome 8:10470359-10470448
RH102027chromosome 8:10557952-10558076
RH104001chromosome 8:10526888-10527052
RH121634chromosome 8:10576434-10576730
RH122237chromosome 8:10746029-10746342
RH12443chromosome 8:10286130-10286302
RH26952chromosome 8:10732041-10732133
RH36675chromosome 8:10622691-10622741
RH65392chromosome 8:10582750-10582939
RH81045chromosome 8:10581327-10581560
SHGC-153612chromosome 8:10260288-10260601
SHGC-154908chromosome 8:10570827-10571169
SHGC-17264chromosome 8:10219721-10219853
SHGC-84859chromosome 8:10425943-10426134
SOX7chromosome 8:10583299-10583420
STS-AA017723chromosome 8:10249920-10250173
WI-11714chromosome 8:10271029-10271155
XKR6chromosome 8:10755465-10755645