A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv25849



Internal ID15838273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24282145..24289621hg38UCSC Ensembl
Outerchr15:24281433..24290431hg38UCSC Ensembl
Innerchr15:24527292..24534768hg19UCSC Ensembl
Outerchr15:24526580..24535578hg19UCSC Ensembl
Innerchr15:22078385..22085861hg18UCSC Ensembl
Outerchr15:22077673..22086671hg18UCSC Ensembl
Innerchr15:22078385..22085861hg17UCSC Ensembl
Outerchr15:22077673..22086671hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg388999
hg198999
hg188999
hg178999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA18860
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)nssv25849
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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