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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26 mapped markers found:

A005O13chromosome X:152916521-152916713
D16S3178chromosome X:152962867-152963068
D16S3203chromosome X:152960695-152960815
DXS7418chromosome X:152982386-152982504
DXS7452chromosome X:152965967-152966122
DXS8087chromosome X:152894370-152894658
G65802chromosome X:153004177-153005118
G65805chromosome X:152949165-152950063
G67205chromosome X:152997684-152998652
G67214chromosome X:153000278-153001196
G69458chromosome X:152973229-152973852
GDB:376683chromosome X:153002612-153002692
GDB:523970chromosome X:152990639-152991175
GDB:524010chromosome X:152990639-152991156
PMC310890P10chromosome X:153006048-153006656
RH18202chromosome X:152961813-152961992
RH70615chromosome X:152980735-152980864
RH70965chromosome X:152915815-152915938
RH71204chromosome X:152960570-152960714
RH71460chromosome X:152980663-152980847
RH79936chromosome X:152966209-152966404
SHGC-152185chromosome X:152894401-152894599
SHGC-31403chromosome X:152944348-152944481
SHGC-59176chromosome X:152873089-152873220
STS-M78874chromosome X:152945567-152945641
UniSTS:99200chromosome X:152990572-152990659