A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3527464



Internal ID18825745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19637241..19926956hg38UCSC Ensembl
Innerchr14:20105479..20395115hg19UCSC Ensembl
Innerchr14:19175240..19464955hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38289716
hg19289637
hg18289716
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049757
Supporting Variants
Samples
Known GenesOR11H2, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3527464
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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