A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26977



Internal ID15844159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21011273..21027666hg38UCSC Ensembl
Outerchr15:21009226..21028166hg38UCSC Ensembl
Innerchr15:21216602..21232995hg19UCSC Ensembl
Outerchr15:21214555..21233495hg19UCSC Ensembl
Innerchr15:19481261..19497654hg18UCSC Ensembl
Outerchr15:19479214..19498154hg18UCSC Ensembl
Innerchr15:19481261..19497654hg17UCSC Ensembl
Outerchr15:19479214..19498154hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3818941
hg1918941
hg1818941
hg1718941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA19221
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)nssv26977
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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