A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592143



Internal ID16379552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162036321..162073611hg38UCSC Ensembl
Innerchr3:161754109..161791399hg19UCSC Ensembl
Innerchr3:163236803..163274093hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3837291
hg1937291
hg1837291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151816
Samples1780862432_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592143
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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