A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820122



Internal ID15238087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:73057729..73061960hg38UCSC Ensembl
Innerchr13:73631867..73636098hg19UCSC Ensembl
Innerchr13:72529868..72534099hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg384232
hg194232
hg184232
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419617
SamplesAK1
Known GenesKLF5
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)nsv820122
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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