A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv958264



Internal ID16252220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:6149725..6184525hg38UCSC Ensembl
Innerchr3:6191412..6226212hg19UCSC Ensembl
Innerchr3:6166412..6201212hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3834801
hg1934801
hg1834801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589513
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv958264
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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