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Human Genome Region REGION64

Assembly:
GRCh37.p13
Location:
chr3:60,558,332-60,952,039
Cytogenetic location:

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Genome issues
Issue ID Status Description Resolution text
HG-1091 Resolved The ambiguous IUPAC bases (M, R) in AF152363.1will be replaced with individual base codes or Ns. The switchpoints have been changed to use the sequence of AC096917.3 through its overlap with AF152363.1 in order to replace ambiguous IUPAC bases (M, R) in AF152363.1 with individual base codes.
Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
JH159131.1 NW_003871058.1 FIX 393,769 113 79
           

REGION64 -- chr3 (NC_000003.11):60,558,332-60,952,039