A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592920



Internal ID16380329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:193059921..193067683hg38UCSC Ensembl
Innerchr3:192777710..192785472hg19UCSC Ensembl
Innerchr3:194260404..194268166hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg387763
hg197763
hg187763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8812n54
Supporting Variantsnssv984543
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592920
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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