A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039155



Internal ID18781686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54953335..55389131hg38UCSC Ensembl
Innerchr11:54720811..55156607hg19UCSC Ensembl
Innerchr11:54477387..54913183hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38435797
hg19435797
hg18435797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1164n100
Supporting Variantsnssv3507124
Samples
Known GenesOR4A15, OR4A16, TRIM48, TRIM51HP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039155
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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