A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21326



Internal ID15841159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20345409..20428755hg38UCSC Ensembl
Outerchr15:20344759..20430310hg38UCSC Ensembl
Innerchr15:20550662..20634008hg19UCSC Ensembl
Outerchr15:20550012..20635563hg19UCSC Ensembl
Innerchr15:18810676..18894022hg18UCSC Ensembl
Outerchr15:18810026..18895577hg18UCSC Ensembl
Innerchr15:18810676..18894022hg17UCSC Ensembl
Outerchr15:18810026..18895577hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3885552
hg1985552
hg1885552
hg1785552
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA19007
Known GenesHERC2P3
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)nssv21326
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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