A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3505955



Internal ID18457550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6761782..6872311hg38UCSC Ensembl
Innerchr11:6783013..6893542hg19UCSC Ensembl
Innerchr11:6739589..6850118hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38110530
hg19110530
hg18110530
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039455
Supporting Variants
Samples
Known GenesOR10A2, OR10A5, OR2AG1, OR2AG2, OR6A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3505955
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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