A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820205



Internal ID15238170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55793542..55832100hg38UCSC Ensembl
Innerchr16:55827454..55866012hg19UCSC Ensembl
Innerchr16:54384955..54423513hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3838559
hg1938559
hg1838559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418727
SamplesAK1
Known GenesCES1
MethodOligo aCGH
AnalysisThe array was scanned with Agilent DNA microarray scanner at 2 micron resolution. The resulting image was extracted by Agilent's Feature Extraction software. The log2 ratios were analyzed using NEXUS software. Each aberration call was manually checked to confirm the accuracy of the calls.
PlatformGSE19651
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nsv820205
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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