A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819750



Internal ID15237715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33392247..33395128hg38UCSC Ensembl
Innerchr20:31980053..31982934hg19UCSC Ensembl
Innerchr20:31443714..31446595hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg382882
hg192882
hg182882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419489
SamplesAK1
Known GenesCDK5RAP1
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)nsv819750
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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