A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23487



Internal ID15484231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32471364..32480218hg38UCSC Ensembl
Outerchr15:32471208..32480854hg38UCSC Ensembl
Innerchr15:32763565..32772419hg19UCSC Ensembl
Outerchr15:32763409..32773055hg19UCSC Ensembl
Innerchr15:30550857..30559711hg18UCSC Ensembl
Outerchr15:30550701..30560347hg18UCSC Ensembl
Innerchr15:30550857..30559711hg17UCSC Ensembl
Outerchr15:30550701..30560347hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg389647
hg199647
hg189647
hg179647
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9238
Supporting Variants
SamplesNA12155
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)nssv23487
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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