A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8871



Internal ID15846783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:105071023..105102781hg38UCSC Ensembl
Outerchr11:104941750..104973508hg19UCSC Ensembl
Outerchr11:104446960..104478718hg18UCSC Ensembl
Outerchr11:104446960..104478718hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3831759
hg1931759
hg1831759
hg1731759
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv20489
SamplesNA19173
Known GenesCARD17
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)nsv8871
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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