A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819360



Internal ID15237325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:137752468..137752870hg38UCSC Ensembl
Innerchr5:137088157..137088559hg19UCSC Ensembl
Innerchr5:137116056..137116458hg18UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg38403
hg19403
hg18403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418939
SamplesAK1
Known GenesHNRNPA0
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)nsv819360
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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