A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv23289



Internal ID15484157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30152561..30399907hg38UCSC Ensembl
Outerchr15:30152060..30400280hg38UCSC Ensembl
Innerchr15:30444764..30692110hg19UCSC Ensembl
Outerchr15:30444263..30692483hg19UCSC Ensembl
Innerchr15:28232056..28479402hg18UCSC Ensembl
Outerchr15:28231555..28479775hg18UCSC Ensembl
Innerchr15:28232056..28479402hg17UCSC Ensembl
Outerchr15:28231555..28479775hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38248221
hg19248221
hg18248221
hg17248221
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9232
Supporting Variants
SamplesNA12155
Known GenesCHRFAM7A, DKFZP434L187
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)nssv23289
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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