A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22447



Internal ID15829856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19966534..20009274hg38UCSC Ensembl
Outerchr15:19966031..20009789hg38UCSC Ensembl
Innerchr15:20171787..20214527hg19UCSC Ensembl
Outerchr15:20171284..20215042hg19UCSC Ensembl
Innerchr15:18431801..18474541hg18UCSC Ensembl
Outerchr15:18431298..18475056hg18UCSC Ensembl
Innerchr15:18431801..18474541hg17UCSC Ensembl
Outerchr15:18431298..18475056hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3843759
hg1943759
hg1843759
hg1743759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA11830
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)nssv22447
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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