A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553224



Internal ID16340633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5117503..5186159hg38UCSC Ensembl
Innerchr11:5138733..5207389hg19UCSC Ensembl
Innerchr11:5095309..5163965hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3868657
hg1968657
hg1868657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv765347
Samples
Known GenesOR52A1, OR52A5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553224
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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