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Human Genome Region SPC25

Assembly:
GRCh38.p14
Location:
chr2:168,830,363-168,937,194
Cytogenetic location:

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 ALT Unavailable Unavailable Unavailable
           

SPC25 -- chr2 (CM000664.2):168,830,363-168,937,194