A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8775



Internal ID15846687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:3641782..3643637hg38UCSC Ensembl
Outerchr11:3663012..3664867hg19UCSC Ensembl
Outerchr11:3619588..3621443hg18UCSC Ensembl
Outerchr11:3619588..3621443hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381856
hg191856
hg181856
hg171856
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18812
SamplesNA07029
Known GenesART5
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)nsv8775
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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