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Human Genome Region REGION86

Assembly:
GRCh37.p13
Location:
chr22:51,203,354-51,244,566
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH806586.1 NW_004070876.1 FIX 43,543 0 2,330
           

REGION86 -- chr22 (NC_000022.10):51,203,354-51,244,566