A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819934



Internal ID15237899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37195303..37196001hg38UCSC Ensembl
Innerchr21:38567604..38568302hg19UCSC Ensembl
Innerchr21:37489474..37490172hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38699
hg19699
hg18699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419062
SamplesAK1
Known GenesTTC3
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)nsv819934
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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