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Human Genome Region REGION56

Assembly:
GRCh37.p13
Location:
chr4:190,828,226-191,044,276
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL877872.1 NW_003571034.1 FIX 297,485 0 31,434
           

REGION56 -- chr4 (NC_000004.11):190,828,226-191,044,276