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Human Genome Region REGION262

Assembly:
GRCh38.p14
Location:
chr3:94,896,163-94,997,637
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KZ559104.1 NW_019805491.1 FIX Unavailable Unavailable Unavailable
           

REGION262 -- chr3 (CM000665.2):94,896,163-94,997,637