A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553378



Internal ID15994101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6757840..6871635hg38UCSC Ensembl
Innerchr11:6779071..6892866hg19UCSC Ensembl
Innerchr11:6735647..6849442hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38113796
hg19113796
hg18113796
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1626n54
Supporting Variantsnssv1174614
SamplesHGDP00807
Known GenesOR10A2, OR10A5, OR2AG1, OR2AG2, OR6A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553378
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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