A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23459



Internal ID15484006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32420012..32441242hg38UCSC Ensembl
Outerchr15:32419310..32441641hg38UCSC Ensembl
Innerchr15:32712213..32733443hg19UCSC Ensembl
Outerchr15:32711511..32733842hg19UCSC Ensembl
Innerchr15:30499505..30520735hg18UCSC Ensembl
Outerchr15:30498803..30521134hg18UCSC Ensembl
Innerchr15:30499505..30520735hg17UCSC Ensembl
Outerchr15:30498803..30521134hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3822332
hg1922332
hg1822332
hg1722332
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9238
Supporting Variants
SamplesNA12155
Known GenesULK4P1, ULK4P2, ULK4P3
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)nssv23459
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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