A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553364



Internal ID16340773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6095546..6100266hg38UCSC Ensembl
Innerchr11:6116776..6121496hg19UCSC Ensembl
Innerchr11:6073352..6078072hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg384721
hg194721
hg184721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1624n54
Supporting Variantsnssv766319
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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