A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040974



Internal ID19130193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54554865..54852259hg38UCSC Ensembl
Innerchr11:51267021..51564415hg19UCSC Ensembl
Innerchr11:51123597..51420991hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38297395
hg19297395
hg18297395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1155n100
Supporting Variantsnssv3506360
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)nsv1040974
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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