A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612396



Internal ID16399805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675712..136829581hg38UCSC Ensembl
Innerchr8:137687955..137841824hg19UCSC Ensembl
Innerchr8:137757137..137911006hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38153870
hg19153870
hg18153870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122264, nssv1122263, nssv1122265
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612396
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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