A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511124



Internal ID18809405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54554865..54762047hg38UCSC Ensembl
Innerchr11:51357233..51564415hg19UCSC Ensembl
Innerchr11:51213809..51420991hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38207183
hg19207183
hg18207183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041340
Supporting Variants
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)nssv3511124
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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