A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv982613



Internal ID16276569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184753117..184763208hg38UCSC Ensembl
Innerchr3:184470905..184480996hg19UCSC Ensembl
Innerchr3:185953599..185963690hg18UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3810092
hg1910092
hg1810092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592683
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)nssv982613
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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