A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039064



Internal ID18781595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55554735..55686088hg38UCSC Ensembl
Innerchr11:55322211..55453564hg19UCSC Ensembl
Innerchr11:55078787..55210140hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38131354
hg19131354
hg18131354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1172n100
Supporting Variantsnssv3507019
Samples
Known GenesOR4C11, OR4C15, OR4C16, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039064
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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