A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589372



Internal ID16030095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2189464..2704772hg38UCSC Ensembl
Innerchr3:2231148..2746456hg19UCSC Ensembl
Innerchr3:2206148..2721456hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38515309
hg19515309
hg18515309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8166n54
Supporting Variantsnssv957908
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589372
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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