A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592914



Internal ID16380323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193059791..193067683hg38UCSC Ensembl
Innerchr3:192777580..192785472hg19UCSC Ensembl
Innerchr3:194260274..194268166hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg387893
hg197893
hg187893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8812n54
Supporting Variantsnssv984512, nssv984514, nssv984509, nssv984510, nssv984513, nssv984511
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592914
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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