A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9237



Internal ID15500463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:31624186..32153679hg38UCSC Ensembl
Outerchr15:31916389..32445880hg19UCSC Ensembl
Outerchr15:29703681..30233172hg18UCSC Ensembl
Outerchr15:29703681..30233172hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38529494
hg19529492
hg18529492
hg17529492
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23402, nssv25204
SamplesNA11830, NA18972
Known GenesCHRNA7, OTUD7A
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)nsv9237
Frequency
Sample Size31
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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