A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589304



Internal ID16030027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:802065..1232032hg38UCSC Ensembl
Innerchr3:843748..1273716hg19UCSC Ensembl
Innerchr3:818748..1248716hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38429968
hg19429969
hg18429969
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8154n54
Supporting Variantsnssv957812
Samples
Known GenesCNTN6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589304
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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