A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046059



Internal ID19135278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54554865..54941169hg38UCSC Ensembl
Innerchr11:51176562..51564415hg19UCSC Ensembl
Innerchr11:51033138..51420991hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38386305
hg19387854
hg18387854
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1155n100
Supporting Variantsnssv3507439, nssv3712380
Samples
Known GenesOR4A5, OR4C46
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046059
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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