A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590111



Internal ID16377520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:40720531..41092119hg38UCSC Ensembl
Innerchr3:40762022..41133610hg19UCSC Ensembl
Innerchr3:40737026..41108614hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38371589
hg19371589
hg18371589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv962387
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590111
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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