A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419417



Internal ID15583201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:46369172..46371489hg38UCSC Ensembl
Innerchr20:44997811..45000128hg19UCSC Ensembl
Innerchr20:44431218..44433535hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg382318
hg192318
hg182318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820217
Supporting Variants
SamplesAK1
Known GenesELMO2
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)nssv1419417
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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