A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957808



Internal ID15905078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:627148..1404826hg38UCSC Ensembl
Innerchr3:668832..1446510hg19UCSC Ensembl
Innerchr3:643832..1421510hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38777679
hg19777679
hg18777679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589297
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)nssv957808
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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