A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9807



Internal ID15847719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:38377499..38388225hg38UCSC Ensembl
Outerchr20:37006141..37016867hg19UCSC Ensembl
Outerchr20:36439555..36450281hg18UCSC Ensembl
Outerchr20:36439555..36450281hg17UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3810727
hg1910727
hg1810727
hg1710727
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25375
SamplesNA18563
Known Genes
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)nsv9807
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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