A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819614



Internal ID15237579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32446792..32447044hg38UCSC Ensembl
Innerchr20:31034595..31034847hg19UCSC Ensembl
Innerchr20:30498256..30498508hg18UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38253
hg19253
hg18253
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419470
SamplesAK1
Known GenesC20orf112
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)nsv819614
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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