A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555086



Internal ID16342495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55927680..55941339hg38UCSC Ensembl
Innerchr11:55695156..55708815hg19UCSC Ensembl
Innerchr11:55451732..55465391hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3813660
hg1913660
hg1813660
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1946n54
Supporting Variantsnssv776850
Samples
Known GenesOR5I1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555086
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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