A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592214



Internal ID16379623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162786533..163004174hg38UCSC Ensembl
Innerchr3:162504321..162721962hg19UCSC Ensembl
Innerchr3:163987015..164204656hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38217642
hg19217642
hg18217642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8679n54
Supporting Variantsnssv977597
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592214
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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