A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10259



Internal ID15498536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:33393610..33395330hg38UCSC Ensembl
Outerchr3:33435102..33436822hg19UCSC Ensembl
Outerchr3:33410106..33411826hg18UCSC Ensembl
Outerchr3:33410106..33411826hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381721
hg191721
hg181721
hg171721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11937
SamplesNA19132
Known GenesUBP1
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)nsv10259
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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