A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25117



Internal ID15834418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24421780..24491638hg38UCSC Ensembl
Outerchr15:24421121..24492004hg38UCSC Ensembl
Innerchr15:24666927..24736785hg19UCSC Ensembl
Outerchr15:24666268..24737151hg19UCSC Ensembl
Innerchr15:22218020..22287878hg18UCSC Ensembl
Outerchr15:22217361..22288244hg18UCSC Ensembl
Innerchr15:22218020..22287878hg17UCSC Ensembl
Outerchr15:22217361..22288244hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3870884
hg1970884
hg1870884
hg1770884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA18517
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)nssv25117
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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