A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819573



Internal ID15584274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23683411..23685263hg38UCSC Ensembl
Innerchr22:24025598..24027450hg19UCSC Ensembl
Innerchr22:22355598..22357450hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg381853
hg191853
hg181853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419343
SamplesAK1
Known GenesGUSBP11
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)nsv819573
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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