A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22335



Internal ID15834866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24427222..24427875hg38UCSC Ensembl
Outerchr15:24426951..24431381hg38UCSC Ensembl
Innerchr15:24672369..24673022hg19UCSC Ensembl
Outerchr15:24672098..24676528hg19UCSC Ensembl
Innerchr15:22223462..22224115hg18UCSC Ensembl
Outerchr15:22223191..22227621hg18UCSC Ensembl
Innerchr15:22223462..22224115hg17UCSC Ensembl
Outerchr15:22223191..22227621hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg384431
hg194431
hg184431
hg174431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA18537
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)nssv22335
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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