A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21276



Internal ID15829757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23180572..23189557hg38UCSC Ensembl
Outerchr15:23178535..23190651hg38UCSC Ensembl
Innerchr15:22683511..22692496hg19UCSC Ensembl
Outerchr15:22682417..22694533hg19UCSC Ensembl
Innerchr15:20234875..20243860hg18UCSC Ensembl
Outerchr15:20233781..20245897hg18UCSC Ensembl
Innerchr15:20234875..20243860hg17UCSC Ensembl
Outerchr15:20233781..20245897hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3812117
hg1912117
hg1812117
hg1712117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9181
Supporting Variants
SamplesNA10863
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)nssv21276
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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