A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045156



Internal ID18787687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:124565356..124705852hg38UCSC Ensembl
Innerchr11:124435252..124575748hg19UCSC Ensembl
Innerchr11:123940462..124080958hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38140497
hg19140497
hg18140497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507972
Samples
Known GenesOR8A1, PANX3, SIAE, SPA17, TBRG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045156
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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