A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174614



Internal ID15529562
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 StatusS
Merged Variantsnsv553378
Supporting Variants
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)nssv1174614
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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