A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20362



Internal ID15838741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24089919..24549071hg38UCSC Ensembl
Outerchr15:24085167..24549275hg38UCSC Ensembl
Innerchr15:24335066..24794218hg19UCSC Ensembl
Outerchr15:24330314..24794422hg19UCSC Ensembl
Innerchr15:21886159..22345311hg18UCSC Ensembl
Outerchr15:21881407..22345515hg18UCSC Ensembl
Innerchr15:21886159..22345311hg17UCSC Ensembl
Outerchr15:21881407..22345515hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38464109
hg19464109
hg18464109
hg17464109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA18942
Known GenesPWRN2
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)nssv20362
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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