A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612321



Internal ID16399730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131446702..131552203hg38UCSC Ensembl
Innerchr8:132458949..132564450hg19UCSC Ensembl
Innerchr8:132528131..132633632hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38105502
hg19105502
hg18105502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12338n54
Supporting Variantsnssv1121516
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612321
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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