A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15263



Internal ID15839312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17570684..17643754hg18UCSC Ensembl
Outerchr5:17570551..17644375hg18UCSC Ensembl
Innerchr5:17570684..17643754hg17UCSC Ensembl
Outerchr5:17570551..17644375hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg1873825
hg1773825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10674
Supporting Variants
SamplesNA18972
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)nssv15263
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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