A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24226



Internal ID15483698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31951706..31974834hg38UCSC Ensembl
Outerchr16:31951186..31975681hg38UCSC Ensembl
Innerchr16:31963027..31986155hg19UCSC Ensembl
Outerchr16:31962507..31987002hg19UCSC Ensembl
Innerchr16:31870528..31893656hg18UCSC Ensembl
Outerchr16:31870008..31894503hg18UCSC Ensembl
Innerchr16:31870528..31893656hg17UCSC Ensembl
Outerchr16:31870008..31894503hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3824496
hg1924496
hg1824496
hg1724496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9439
Supporting Variants
SamplesNA12155
Known Genes
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)nssv24226
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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