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Human Genome Region REGION22

Assembly:
GRCh38.p14
Location:
chr12:57,932,737-58,092,755
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383550.2 NW_003315939.2 ALT Unavailable Unavailable Unavailable
           

REGION22 -- chr12 (CM000674.2):57,932,737-58,092,755