A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611810



Internal ID16399219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:99196738..99289393hg38UCSC Ensembl
Innerchr8:100208966..100301621hg19UCSC Ensembl
Innerchr8:100278142..100370797hg18UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3892656
hg1992656
hg1892656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1118157
Samples
Known GenesVPS13B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611810
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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