A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19660



Internal ID15485212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34425141..34425951hg38UCSC Ensembl
Outerchr15:34424505..34427415hg38UCSC Ensembl
Innerchr15:34717342..34718152hg19UCSC Ensembl
Outerchr15:34716706..34719616hg19UCSC Ensembl
Innerchr15:32504634..32505444hg18UCSC Ensembl
Outerchr15:32503998..32506908hg18UCSC Ensembl
Innerchr15:32504634..32505444hg17UCSC Ensembl
Outerchr15:32503998..32506908hg17UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382911
hg192911
hg182911
hg172911
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9241
Supporting Variants
SamplesNA12802
Known GenesGOLGA8A
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)nssv19660
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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