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Human Genome Region SPC25

Assembly:
GRCh37.p13
Location:
chr2:169,686,873-169,793,704
Cytogenetic location:

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No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
GL383522.1 NW_003315909.1 NOVEL 123,821 55 17,002
           

SPC25 -- chr2 (NC_000002.11):169,686,873-169,793,704