A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555231



Internal ID16342640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:66944758..66945393hg38UCSC Ensembl
Innerchr11:66712229..66712864hg19UCSC Ensembl
Innerchr11:66468805..66469440hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38636
hg19636
hg18636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1972n54
Supporting Variantsnssv778536
Samples
Known GenesPC
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555231
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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