A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589370



Internal ID16030093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2167148..2359283hg38UCSC Ensembl
Innerchr3:2208832..2400967hg19UCSC Ensembl
Innerchr3:2183832..2375967hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38192136
hg19192136
hg18192136
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957906
Samples
Known GenesCNTN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589370
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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