A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23515



Internal ID15484038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32504559..32514221hg38UCSC Ensembl
Outerchr15:32500403..32514832hg38UCSC Ensembl
Innerchr15:32796760..32806422hg19UCSC Ensembl
Outerchr15:32792604..32807033hg19UCSC Ensembl
Innerchr15:30584052..30593714hg18UCSC Ensembl
Outerchr15:30579896..30594325hg18UCSC Ensembl
Innerchr15:30584052..30593714hg17UCSC Ensembl
Outerchr15:30579896..30594325hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3814430
hg1914430
hg1814430
hg1714430
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)nssv23515
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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