A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22259



Internal ID15843001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23205682..23207265hg38UCSC Ensembl
Outerchr15:23205187..23207421hg38UCSC Ensembl
Innerchr15:22665803..22667386hg19UCSC Ensembl
Outerchr15:22665647..22667881hg19UCSC Ensembl
Innerchr15:20217167..20218750hg18UCSC Ensembl
Outerchr15:20217011..20219245hg18UCSC Ensembl
Innerchr15:20217167..20218750hg17UCSC Ensembl
Outerchr15:20217011..20219245hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382235
hg192235
hg182235
hg172235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9181
Supporting Variants
SamplesNA19173
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)nssv22259
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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