A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22687



Internal ID15830768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20359383..20371100hg38UCSC Ensembl
Outerchr15:20359035..20371691hg38UCSC Ensembl
Innerchr15:20564636..20576353hg19UCSC Ensembl
Outerchr15:20564288..20576944hg19UCSC Ensembl
Innerchr15:18824650..18836367hg18UCSC Ensembl
Outerchr15:18824302..18836958hg18UCSC Ensembl
Innerchr15:18824650..18836367hg17UCSC Ensembl
Outerchr15:18824302..18836958hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3812657
hg1912657
hg1812657
hg1712657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12155
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)nssv22687
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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