A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820074



Internal ID15238039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:204241510..204241960hg38UCSC Ensembl
Innerchr1:204210638..204211088hg19UCSC Ensembl
Innerchr1:202477261..202477711hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38451
hg19451
hg18451
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418957
SamplesAK1
Known GenesPLEKHA6
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)nsv820074
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