Skip navigation and go to main content

Human Genome Region REGION237

Assembly:
GRCh38.p14
Location:
chr17:52,434,177-52,673,566
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KV766197.1 NW_017363818.1 NOVEL Unavailable Unavailable Unavailable
           

REGION237 -- chr17 (CM000679.2):52,434,177-52,673,566