A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21534



Internal ID15840038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28638141..28639660hg38UCSC Ensembl
Outerchr15:28637791..28640089hg38UCSC Ensembl
Innerchr15:28883287..28884806hg19UCSC Ensembl
Outerchr15:28882937..28885235hg19UCSC Ensembl
Innerchr15:26682328..26683847hg18UCSC Ensembl
Outerchr15:26681978..26684276hg18UCSC Ensembl
Innerchr15:26682328..26683847hg17UCSC Ensembl
Outerchr15:26681978..26684276hg17UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382299
hg192299
hg182299
hg172299
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9216
Supporting Variants
SamplesNA18975
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)nssv21534
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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