A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589619



Internal ID16030342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8740720..8816277hg38UCSC Ensembl
Innerchr3:8782406..8857963hg19UCSC Ensembl
Innerchr3:8757406..8832963hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3875558
hg1975558
hg1875558
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv958859
Samples
Known GenesCAV3, OXTR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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