A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820103



Internal ID15584804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:118256004..118261206hg38UCSC Ensembl
Innerchr2:119013580..119018782hg19UCSC Ensembl
Innerchr2:118730050..118735252hg18UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg385203
hg195203
hg185203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419691
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)nsv820103
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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