A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554878



Internal ID15995601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602849..55692619hg38UCSC Ensembl
Innerchr11:55370325..55460095hg19UCSC Ensembl
Innerchr11:55126901..55216671hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3889771
hg1989771
hg1889771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1916n54
Supporting Variantsnssv775961
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554878
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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