A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156828



Internal ID15876612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:31288942..31316342hg38UCSC Ensembl
Innerchr8:31146458..31173858hg19UCSC Ensembl
Innerchr8:31266000..31293400hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3827401
hg1927401
hg1827401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv610879
Supporting Variants
SamplesHGDP00868
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156828
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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