A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25038



Internal ID15483835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:70111551..70113476hg38UCSC Ensembl
Outerchr16:70110189..70113800hg38UCSC Ensembl
Innerchr16:70145454..70147379hg19UCSC Ensembl
Outerchr16:70144092..70147703hg19UCSC Ensembl
Innerchr16:68702955..68704880hg18UCSC Ensembl
Outerchr16:68701593..68705204hg18UCSC Ensembl
Innerchr16:68702955..68704880hg17UCSC Ensembl
Outerchr16:68701593..68705204hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg383612
hg193612
hg183612
hg173612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9455
Supporting Variants
SamplesNA12155
Known GenesPDPR
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nssv25038
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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