A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv960106



Internal ID16254062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:22549197..22590102hg38UCSC Ensembl
Innerchr3:22590688..22631593hg19UCSC Ensembl
Innerchr3:22565692..22606597hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3840906
hg1940906
hg1840906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589944
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)nssv960106
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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