A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612322



Internal ID16399731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131446702..131566427hg38UCSC Ensembl
Innerchr8:132458949..132578674hg19UCSC Ensembl
Innerchr8:132528131..132647856hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38119726
hg19119726
hg18119726
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12338n54
Supporting Variantsnssv1156641
SamplesHGDP01279
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612322
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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