A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21866



Internal ID15841104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24421780..24477479hg38UCSC Ensembl
Outerchr15:24421121..24477754hg38UCSC Ensembl
Innerchr15:24666927..24722626hg19UCSC Ensembl
Outerchr15:24666268..24722901hg19UCSC Ensembl
Innerchr15:22218020..22273719hg18UCSC Ensembl
Outerchr15:22217361..22273994hg18UCSC Ensembl
Innerchr15:22218020..22273719hg17UCSC Ensembl
Outerchr15:22217361..22273994hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3856634
hg1956634
hg1856634
hg1756634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9195
Supporting Variants
SamplesNA19007
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)nssv21866
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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