A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556450



Internal ID16343859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116600547..116632927hg38UCSC Ensembl
Innerchr11:116471264..116503644hg19UCSC Ensembl
Innerchr11:115976474..116008854hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3832381
hg1932381
hg1832381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784585
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556450
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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