A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554867



Internal ID15995590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602849..55650706hg38UCSC Ensembl
Innerchr11:55370325..55418182hg19UCSC Ensembl
Innerchr11:55126901..55174758hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3847858
hg1947858
hg1847858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1914n54
Supporting Variantsnssv775928
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554867
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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