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Human Genome Region REGION206

Assembly:
GRCh38.p14
Location:
chr12:12,031,003-12,572,035
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KN538369.1 NW_011332696.1 FIX Unavailable Unavailable Unavailable
           

REGION206 -- chr12 (CM000674.2):12,031,003-12,572,035