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Human Genome Region REGION190

Assembly:
GRCh38.p14
Location:
chr1:112,909,422-113,029,606
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KN196474.1 NW_009646196.1 FIX Unavailable Unavailable Unavailable
           

REGION190 -- chr1 (CM000663.2):112,909,422-113,029,606