A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8869



Internal ID15846781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:104853878..104889310hg38UCSC Ensembl
Outerchr11:104724605..104760037hg19UCSC Ensembl
Outerchr11:104229815..104265247hg18UCSC Ensembl
Outerchr11:104229815..104265247hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3835433
hg1935433
hg1835433
hg1735433
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv22543, nssv23182
SamplesNA18504, NA18517
Known GenesCASP12
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)nsv8869
Frequency
Sample Size31
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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