A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv22269



Internal ID15831512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20074311..20096058hg38UCSC Ensembl
Outerchr15:20073972..20096681hg38UCSC Ensembl
Innerchr15:20279564..20301311hg19UCSC Ensembl
Outerchr15:20279225..20301934hg19UCSC Ensembl
Innerchr15:18539578..18561325hg18UCSC Ensembl
Outerchr15:18539239..18561948hg18UCSC Ensembl
Innerchr15:18539578..18561325hg17UCSC Ensembl
Outerchr15:18539239..18561948hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg3822710
hg1922710
hg1822710
hg1722710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA12740
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)nssv22269
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer