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Human Genome Region REGION96

Assembly:
GRCh37.p13
Location:
chrX:139,986,363-140,891,303
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH806598.1 NW_004070888.1 FIX 899,320 896 6,835
           

REGION96 -- chrX (NC_000023.10):139,986,363-140,891,303