A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819067



Internal ID15583768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:203034052..203039204hg38UCSC Ensembl
Innerchr2:203898775..203903927hg19UCSC Ensembl
Innerchr2:203607020..203612172hg18UCSC Ensembl
Cytoband2q33.2
Allele length
AssemblyAllele length
hg385153
hg195153
hg185153
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419685
SamplesAK1
Known GenesNBEAL1
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)nsv819067
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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