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Human Genome Region REGION20

Assembly:
GRCh38.p14
Location:
chr12:126,227,198-126,405,474
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383551.1 NW_003315940.1 ALT Unavailable Unavailable Unavailable
           

REGION20 -- chr12 (CM000674.2):126,227,198-126,405,474