A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2798665



Internal ID15268200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19734447..19952765hg38UCSC Ensembl
Innerchr14:20202606..20420924hg19UCSC Ensembl
Innerchr14:19272446..19490764hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38218319
hg19218319
hg18218319
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514728
Supporting Variants
SamplesNA11919
Known GenesOR4K1, OR4K2, OR4K5, OR4M1, OR4N2, OR4Q3
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2798665
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer