A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553223



Internal ID16340632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5094898..5128102hg38UCSC Ensembl
Innerchr11:5116128..5149332hg19UCSC Ensembl
Innerchr11:5072704..5105908hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3833205
hg1933205
hg1833205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv765346
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553223
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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