A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv21746



Internal ID15841117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24261163..24290632hg38UCSC Ensembl
Outerchr15:24260863..24292235hg38UCSC Ensembl
Innerchr15:24506310..24535779hg19UCSC Ensembl
Outerchr15:24506010..24537382hg19UCSC Ensembl
Innerchr15:22057403..22086872hg18UCSC Ensembl
Outerchr15:22057103..22088475hg18UCSC Ensembl
Innerchr15:22057403..22086872hg17UCSC Ensembl
Outerchr15:22057103..22088475hg17UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3831373
hg1931373
hg1831373
hg1731373
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)nssv21746
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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