A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3502827



Internal ID18801108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:54567886..54924229hg38UCSC Ensembl
Innerchr11:51195051..51551394hg19UCSC Ensembl
Innerchr11:51051627..51407970hg18UCSC Ensembl
Cytoband11p11.11
Allele length
AssemblyAllele length
hg38356344
hg19356344
hg18356344
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1036334
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)nssv3502827
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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