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Human Genome Region REGION40

Assembly:
GRCh38.p14
Location:
chr20:17,771,102-17,893,471
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383577.2 NW_003315966.2 ALT Unavailable Unavailable Unavailable
           

REGION40 -- chr20 (CM000682.2):17,771,102-17,893,471