A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556038



Internal ID16343447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98695864..98804190hg38UCSC Ensembl
Innerchr11:98566594..98674920hg19UCSC Ensembl
Innerchr11:98071804..98180130hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38108327
hg19108327
hg18108327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2113n54
Supporting Variantsnssv781713
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556038
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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