A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609737



Internal ID16397146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:3462226..3475605hg38UCSC Ensembl
Innerchr8:3319748..3333127hg19UCSC Ensembl
Innerchr8:3307156..3320535hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg3813380
hg1913380
hg1813380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156110
SamplesHGDP00160
Known GenesCSMD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609737
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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