A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711998



Internal ID19010279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19732012..19951100hg38UCSC Ensembl
Innerchr14:20200171..20419259hg19UCSC Ensembl
Innerchr14:19270011..19489099hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38219089
hg19219089
hg18219089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047940
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)nssv3711998
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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