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Human Genome Region REGION50

Assembly:
GRCh38.p14
Location:
chr12:10,001-173,298
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL877875.1 NW_003571049.1 ALT Unavailable Unavailable Unavailable
           

REGION50 -- chr12 (CM000674.2):10,001-173,298