A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2819532



Internal ID15383051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15883901..15884296hg38UCSC Ensembl
Innerchr16:15977758..15978153hg19UCSC Ensembl
Innerchr16:15885259..15885654hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38396
hg19396
hg18396
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514795
Supporting Variants
SamplesNA19101
Known GenesFOPNL
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2819532
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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