A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612434



Internal ID16399843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136692489..136864159hg38UCSC Ensembl
Innerchr8:137704732..137876402hg19UCSC Ensembl
Innerchr8:137773914..137945584hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38171671
hg19171671
hg18171671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12343n54
Supporting Variantsnssv1122412
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612434
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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