A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv27137



Internal ID15844319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24853002..24854612hg38UCSC Ensembl
Outerchr15:24852579..24855381hg38UCSC Ensembl
Innerchr15:25098149..25099759hg19UCSC Ensembl
Outerchr15:25097726..25100528hg19UCSC Ensembl
Innerchr15:22649242..22650852hg18UCSC Ensembl
Outerchr15:22648819..22651621hg18UCSC Ensembl
Innerchr15:22649242..22650852hg17UCSC Ensembl
Outerchr15:22648819..22651621hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg382803
hg192803
hg182803
hg172803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9198
Supporting Variants
SamplesNA19221
Known GenesSNRPN
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)nssv27137
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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