A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553178



Internal ID16340587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4785642..4887770hg38UCSC Ensembl
Innerchr11:4806872..4909000hg19UCSC Ensembl
Innerchr11:4763448..4865576hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38102129
hg19102129
hg18102129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1587n54
Supporting Variantsnssv764674, nssv764672, nssv764673
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)nsv553178
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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