A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819515



Internal ID15584216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:68580294..68592452hg38UCSC Ensembl
Innerchr3:68629445..68641603hg19UCSC Ensembl
Innerchr3:68712135..68724293hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3812159
hg1912159
hg1812159
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418628
SamplesAK1
Known Genes
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)nsv819515
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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