A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv960096



Internal ID15907366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21943925..22006442hg38UCSC Ensembl
Innerchr3:21985417..22047934hg19UCSC Ensembl
Innerchr3:21960421..22022938hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3862518
hg1962518
hg1862518
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589932
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)nssv960096
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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