A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764670



Internal ID16058626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4785476..4887770hg38UCSC Ensembl
Innerchr11:4806706..4909000hg19UCSC Ensembl
Innerchr11:4763282..4865576hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38102295
hg19102295
hg18102295
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553176
Supporting Variants
Samples
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764670
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer