A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv20642



Internal ID15827564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19662785..19796797hg17UCSC Ensembl
Outerchr15:19662119..19797235hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17135117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv9179
Supporting Variants
SamplesNA07029
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)nssv20642
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer