Skip navigation and go to main content

Human Genome Region REGION196

Assembly:
GRCh38.p14
Location:
chr12:17,717,409-17,928,910
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KN196482.1 NW_009646204.1 FIX Unavailable Unavailable Unavailable
           

REGION196 -- chr12 (CM000674.2):17,717,409-17,928,910