A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556044



Internal ID16343453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98928537..99010412hg38UCSC Ensembl
Innerchr11:98799267..98881142hg19UCSC Ensembl
Innerchr11:98304477..98386352hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3881876
hg1981876
hg1881876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv781718
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556044
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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