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Human Genome Region REGION229

Assembly:
GRCh38.p14
Location:
chr1:103,909,381-104,045,121
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
KQ458382.1 NW_014040925.1 NOVEL Unavailable Unavailable Unavailable
           

REGION229 -- chr1 (CM000663.2):103,909,381-104,045,121