A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530724



Internal ID18829005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20069592..20201081hg38UCSC Ensembl
Innerchr14:20537751..20669240hg19UCSC Ensembl
Innerchr14:19607591..19739080hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38131490
hg19131490
hg18131490
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037890
Supporting Variants
Samples
Known GenesOR11G2, OR4K17, OR4N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3530724
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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