A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv26997



Internal ID15844179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19663241..19790503hg17UCSC Ensembl
Outerchr15:19662785..19790877hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17128093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA19221
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)nssv26997
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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