A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590737



Internal ID16378146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:79237651..79361864hg38UCSC Ensembl
Innerchr3:79286801..79411014hg19UCSC Ensembl
Innerchr3:79369491..79493704hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38124214
hg19124214
hg18124214
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8394n54
Supporting Variantsnssv965829
Samples
Known GenesROBO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590737
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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