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Human Genome Region REGION236

Assembly:
GRCh38.p14
Location:
chr4:154,079,465-154,493,046
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KV766193.1 NW_017363814.1 NOVEL Unavailable Unavailable Unavailable
           

REGION236 -- chr4 (CM000666.2):154,079,465-154,493,046