A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556462



Internal ID16343871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:117814628..117819828hg38UCSC Ensembl
Innerchr11:117685343..117690543hg19UCSC Ensembl
Innerchr11:117190553..117195753hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385201
hg195201
hg185201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784609
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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