A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528793



Internal ID18827074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19732012..19950786hg38UCSC Ensembl
Innerchr14:20200171..20418945hg19UCSC Ensembl
Innerchr14:19270011..19488785hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38218775
hg19218775
hg18218775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047396
Supporting Variants
Samples
Known GenesOR4K1, 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)nssv3528793
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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