A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957807



Internal ID15905077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:627148..1308450hg38UCSC Ensembl
Innerchr3:668832..1350134hg19UCSC Ensembl
Innerchr3:643832..1325134hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38681303
hg19681303
hg18681303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589296
Supporting Variants
Samples
Known GenesCNTN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957807
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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