A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819569



Internal ID15237534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111756761..111758479hg38UCSC Ensembl
Innerchr5:111092458..111094176hg19UCSC Ensembl
Innerchr5:111120357..111122075hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg381719
hg191719
hg181719
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419312
SamplesAK1
Known GenesNREP
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)nsv819569
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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