A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv960111



Internal ID15907381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24652530..24775483hg38UCSC Ensembl
Innerchr3:24694021..24816974hg19UCSC Ensembl
Innerchr3:24669025..24791978hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg38122954
hg19122954
hg18122954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589950
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)nssv960111
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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