A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21806



Internal ID15841110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24366552..24371918hg38UCSC Ensembl
Outerchr15:24366267..24374457hg38UCSC Ensembl
Innerchr15:24611699..24617065hg19UCSC Ensembl
Outerchr15:24611414..24619604hg19UCSC Ensembl
Innerchr15:22162792..22168158hg18UCSC Ensembl
Outerchr15:22162507..22170697hg18UCSC Ensembl
Innerchr15:22162792..22168158hg17UCSC Ensembl
Outerchr15:22162507..22170697hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg388191
hg198191
hg188191
hg178191
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)nssv21806
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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