A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819131



Internal ID15237096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:38037529..38044812hg38UCSC Ensembl
Innerchr3:38079020..38086303hg19UCSC Ensembl
Innerchr3:38054024..38061307hg18UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg387284
hg197284
hg187284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419818
SamplesAK1
Known GenesDLEC1
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)nsv819131
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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