A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679110



Internal ID15415762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:37496412..37547423hg38UCSC Ensembl
Innerchr13:38070549..38121560hg19UCSC Ensembl
Innerchr13:36968549..37019560hg18UCSC Ensembl
Innerchr13:36968549..37019560hg17UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3851012
hg1951012
hg1851012
hg1751012
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517476
Supporting Variants
Samples
Known GenesLINC00547
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679110
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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