A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047882



Internal ID18790413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55473527..55618909hg38UCSC Ensembl
Innerchr11:55241003..55386385hg19UCSC Ensembl
Innerchr11:54997579..55142961hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38145383
hg19145383
hg18145383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1170n100
Supporting Variantsnssv3712396
Samples
Known GenesOR4C11, OR4C15, OR4C16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047882
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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