A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819680



Internal ID15584381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:22048731..22792092hg38UCSC Ensembl
Innerchr2:22271603..23014964hg19UCSC Ensembl
Innerchr2:22125108..22868469hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38743362
hg19743362
hg18743362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4n43
Supporting Variantsnssv1418807
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)nsv819680
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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