A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052076



Internal ID18794607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:48056312..48680997hg38UCSC Ensembl
Innerchr11:48077864..48702549hg19UCSC Ensembl
Innerchr11:48034440..48659125hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38624686
hg19624686
hg18624686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1112n100
Supporting Variantsnssv3522021
Samples
Known GenesOR4A47, OR4B1, OR4C3, OR4C45, OR4S1, OR4X1, OR4X2, PTPRJ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052076
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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