A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9829



Internal ID15501055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63918561..63920466hg38UCSC Ensembl
Outerchr20:62549914..62551819hg19UCSC Ensembl
Outerchr20:62020358..62022263hg18UCSC Ensembl
Outerchr20:62020358..62022263hg17UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381906
hg191906
hg181906
hg171906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv25573
SamplesNA18564
Known GenesDNAJC5, MIR941-1, MIR941-2, MIR941-3, MIR941-4
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)nsv9829
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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