A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524732



Internal ID15452025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20052901..20126230hg38UCSC Ensembl
Innerchr14:20521060..20594389hg19UCSC Ensembl
Innerchr14:19590900..19664229hg18UCSC Ensembl
Innerchr14:19590900..19664229hg17UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3873330
hg1973330
hg1873330
hg1773330
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv122n21
Supporting Variantsnssv700723
Samples
Known GenesOR4K17, OR4L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524732
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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