A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510692



Internal ID18462287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55584048..55679977hg38UCSC Ensembl
Innerchr11:55351524..55447453hg19UCSC Ensembl
Innerchr11:55108100..55204029hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3895930
hg1995930
hg1895930
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048215
Supporting Variants
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3510692
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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