A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819099



Internal ID15237064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:179326927..179328770hg38UCSC Ensembl
Innerchr5:178753928..178755771hg19UCSC Ensembl
Innerchr5:178686534..178688377hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg381844
hg191844
hg181844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419339
SamplesAK1
Known GenesADAMTS2
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)nsv819099
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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