A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819083



Internal ID15237048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10327806..10328399hg38UCSC Ensembl
Innerchr3:10369490..10370083hg19UCSC Ensembl
Innerchr3:10344490..10345083hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38594
hg19594
hg18594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419018
SamplesAK1
Known GenesATP2B2
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)nsv819083
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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