A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589367



Internal ID16030090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2030247..2478272hg38UCSC Ensembl
Innerchr3:2071931..2519956hg19UCSC Ensembl
Innerchr3:2046931..2494956hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38448026
hg19448026
hg18448026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8164n54
Supporting Variantsnssv1152437
Samples1780862435_A
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589367
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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