A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10258



Internal ID15845221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:33378596..33381744hg38UCSC Ensembl
Outerchr3:33420088..33423236hg19UCSC Ensembl
Outerchr3:33395092..33398240hg18UCSC Ensembl
Outerchr3:33395092..33398240hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg383149
hg193149
hg183149
hg173149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11508
SamplesNA18564
Known GenesFBXL2
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)nsv10258
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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