A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv967323



Internal ID16261279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:84151382..84511633hg38UCSC Ensembl
Innerchr3:84200533..84560784hg19UCSC Ensembl
Innerchr3:84283223..84643474hg18UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg38360252
hg19360252
hg18360252
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv590848
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)nssv967323
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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