A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696362



Internal ID15433014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:43254034..43310544hg38UCSC Ensembl
Innerchr13:43828170..43884680hg19UCSC Ensembl
Innerchr13:42726170..42782680hg18UCSC Ensembl
Innerchr13:42726170..42782680hg17UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3856511
hg1956511
hg1856511
hg1756511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518904
Supporting Variants
Samples
Known GenesENOX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696362
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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