A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22658



Internal ID15830763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20185581..20224769hg38UCSC Ensembl
Outerchr15:20184926..20225453hg38UCSC Ensembl
Innerchr15:20390834..20430022hg19UCSC Ensembl
Outerchr15:20390179..20430706hg19UCSC Ensembl
Innerchr15:18650848..18690036hg18UCSC Ensembl
Outerchr15:18650193..18690720hg18UCSC Ensembl
Innerchr15:18650848..18690036hg17UCSC Ensembl
Outerchr15:18650193..18690720hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3840528
hg1940528
hg1840528
hg1740528
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)nssv22658
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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