A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589366



Internal ID16030089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1907610..2384571hg38UCSC Ensembl
Innerchr3:1949294..2426255hg19UCSC Ensembl
Innerchr3:1924294..2401255hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38476962
hg19476962
hg18476962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8164n54
Supporting Variantsnssv957905
Samples
Known GenesCNTN4, CNTN4-AS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589366
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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