A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2820694



Internal ID15248453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70114836..70162524hg38UCSC Ensembl
Innerchr16:70148739..70196427hg19UCSC Ensembl
Innerchr16:68706240..68753928hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3847689
hg1947689
hg1847689
Variant TypeCNV gain
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514810
Supporting Variants
SamplesNA07346
Known GenesPDPR
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2820694
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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