A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590112



Internal ID16377521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:41043968..41132808hg38UCSC Ensembl
Innerchr3:41085459..41174299hg19UCSC Ensembl
Innerchr3:41060463..41149303hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3888841
hg1988841
hg1888841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962388
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590112
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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