A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv24837



Internal ID15834283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20517098..20517714hg38UCSC Ensembl
Outerchr15:20516742..20517903hg38UCSC Ensembl
Innerchr15:20722338..20722954hg19UCSC Ensembl
Outerchr15:20721982..20723143hg19UCSC Ensembl
Innerchr15:18982352..18982968hg18UCSC Ensembl
Outerchr15:18981996..18983157hg18UCSC Ensembl
Innerchr15:18982352..18982968hg17UCSC Ensembl
Outerchr15:18981996..18983157hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381162
hg191162
hg181162
hg171162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18517
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)nssv24837
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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