A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9245



Internal ID15500471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:42149651..42161374hg38UCSC Ensembl
Outerchr15:42441849..42453572hg19UCSC Ensembl
Outerchr15:40229141..40240864hg18UCSC Ensembl
Outerchr15:40229141..40240864hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3811724
hg1911724
hg1811724
hg1711724
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv27468
SamplesNA19221
Known GenesPLA2G4F, VPS39
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)nsv9245
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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