A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9266



Internal ID15847178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:53493230..53498112hg38UCSC Ensembl
Outerchr15:53785427..53790309hg19UCSC Ensembl
Outerchr15:51572719..51577601hg18UCSC Ensembl
Outerchr15:51572719..51577601hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg384883
hg194883
hg184883
hg174883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27500
SamplesNA19221
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)nsv9266
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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