A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555075



Internal ID16342484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55692619..55836936hg38UCSC Ensembl
Innerchr11:55460095..55604412hg19UCSC Ensembl
Innerchr11:55216671..55360988hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38144318
hg19144318
hg18144318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1941n54
Supporting Variantsnssv776843
Samples
Known GenesOR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555075
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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