A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22226



Internal ID15494381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30424653..30512606hg38UCSC Ensembl
Outerchr15:30424066..30513276hg38UCSC Ensembl
Innerchr15:30716856..30804809hg19UCSC Ensembl
Outerchr15:30716269..30805479hg19UCSC Ensembl
Innerchr15:28504148..28592101hg18UCSC Ensembl
Outerchr15:28503561..28592771hg18UCSC Ensembl
Innerchr15:28504148..28592101hg17UCSC Ensembl
Outerchr15:28503561..28592771hg17UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3889211
hg1989211
hg1889211
hg1789211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9232
Supporting Variants
SamplesNA19007
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)nssv22226
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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