A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553180



Internal ID16340589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4786997..4850251hg38UCSC Ensembl
Innerchr11:4808227..4871481hg19UCSC Ensembl
Innerchr11:4764803..4828057hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3863255
hg1963255
hg1863255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1588n54
Supporting Variantsnssv764676
Samples
Known GenesOR51F2, OR51S1, OR52R1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553180
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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