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Human Genome Region REGION34

Assembly:
GRCh37.p13
Location:
chr18:70,600,357-70,692,016
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383568.1 NW_003315957.1 NOVEL 104,552 231 12,901
           

REGION34 -- chr18 (NC_000018.9):70,600,357-70,692,016