A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2818565



Internal ID15455375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:18596865..18664153hg38UCSC Ensembl
Innerchr16:18608187..18675475hg19UCSC Ensembl
Innerchr16:18515688..18582976hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3867289
hg1967289
hg1867289
Variant TypeCNV gain
Copy Number5
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514796
Supporting Variants
SamplesNA21514
Known GenesABCC6P1
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2818565
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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