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Human Genome Region REGION88

Assembly:
GRCh37.p13
Location:
chrX:62,203,738-63,086,230
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH806591.1 NW_004070881.1 FIX 882,083 33 7,747
           

REGION88 -- chrX (NC_000023.10):62,203,738-63,086,230