A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20059



Internal ID15836976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:70736294..70759897hg38UCSC Ensembl
Outerchr15:70735603..70761475hg38UCSC Ensembl
Innerchr15:71028633..71052236hg19UCSC Ensembl
Outerchr15:71027942..71053814hg19UCSC Ensembl
Innerchr15:68815687..68839290hg18UCSC Ensembl
Outerchr15:68814996..68840868hg18UCSC Ensembl
Innerchr15:68815687..68839290hg17UCSC Ensembl
Outerchr15:68814996..68840868hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3825873
hg1925873
hg1825873
hg1725873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9274
Supporting Variants
SamplesNA18572
Known GenesUACA
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)nssv20059
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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