A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039396



Internal ID19128615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19732012..19905991hg38UCSC Ensembl
Innerchr14:20200171..20374150hg19UCSC Ensembl
Innerchr14:19270011..19443990hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38173980
hg19173980
hg18173980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1778n100
Supporting Variantsnssv3711975
Samples
Known GenesOR4K2, 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)nsv1039396
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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