A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052156



Internal ID18794687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5982198..6086548hg38UCSC Ensembl
Innerchr11:6003428..6107778hg19UCSC Ensembl
Innerchr11:5960004..6064354hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38104351
hg19104351
hg18104351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1054n100
Supporting Variantsnssv3708503
Samples
Known GenesOR52L1, OR56A1, OR56A4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052156
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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