A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048857



Internal ID18791388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6761161..6872311hg38UCSC Ensembl
Innerchr11:6782392..6893542hg19UCSC Ensembl
Innerchr11:6738968..6850118hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38111151
hg19111151
hg18111151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1056n100
Supporting Variantsnssv3518032, nssv3708506
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)nsv1048857
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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