A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554852



Internal ID15995575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55602150..55682240hg38UCSC Ensembl
Innerchr11:55369626..55449716hg19UCSC Ensembl
Innerchr11:55126202..55206292hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3880091
hg1980091
hg1880091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1909n54
Supporting Variantsnssv775688
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)nsv554852
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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