A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682672



Internal ID15072638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:33046843..33568722hg38UCSC Ensembl
Innerchr11:33068389..33590268hg19UCSC Ensembl
Innerchr11:33024965..33546844hg18UCSC Ensembl
Innerchr11:33024965..33546844hg17UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38521880
hg19521880
hg18521880
hg17521880
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521130
Supporting Variants
Samples
Known GenesCSTF3, CSTF3-AS1, HIPK3, KIAA1549L, LINC00294, TCP11L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682672
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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