A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13285



Internal ID15840913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17570551..17645194hg18UCSC Ensembl
Outerchr5:17569932..17645615hg18UCSC Ensembl
Innerchr5:17570551..17645194hg17UCSC Ensembl
Outerchr5:17569932..17645615hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg1875684
hg1775684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10674
Supporting Variants
SamplesNA18980
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)nssv13285
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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