A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv612340



Internal ID16399749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136043623..136105469hg38UCSC Ensembl
Innerchr8:137055866..137117712hg19UCSC Ensembl
Innerchr8:137125048..137186894hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3861847
hg1961847
hg1861847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1121529
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv612340
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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