A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611019



Internal ID16398428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39381083..39457032hg38UCSC Ensembl
Innerchr8:39238602..39314551hg19UCSC Ensembl
Innerchr8:39357759..39433708hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3875950
hg1975950
hg1875950
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12096n54
Supporting Variantsnssv1111100
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611019
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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