A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21618



Internal ID15836562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20063783..20069785hg38UCSC Ensembl
Outerchr15:20062351..20070509hg38UCSC Ensembl
Innerchr15:20269036..20275038hg19UCSC Ensembl
Outerchr15:20267604..20275762hg19UCSC Ensembl
Innerchr15:18529050..18535052hg18UCSC Ensembl
Outerchr15:18527618..18535776hg18UCSC Ensembl
Innerchr15:18529050..18535052hg17UCSC Ensembl
Outerchr15:18527618..18535776hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg388159
hg198159
hg188159
hg178159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA18564
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)nssv21618
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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