A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174292



Internal ID15853269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4794118..4895859hg38UCSC Ensembl
Innerchr11:4815348..4917089hg19UCSC Ensembl
Innerchr11:4771924..4873665hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38101742
hg19101742
hg18101742
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553184
Supporting Variants
Samples1780854058_A
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)nssv1174292
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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