A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589297



Internal ID16030020
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 StatusM
Merged Variantsdgv8153n54
Supporting Variantsnssv957808
Samples
Known GenesCNTN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589297
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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