A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819620



Internal ID15584321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:43422886..43423422hg38UCSC Ensembl
Innerchr12:43816689..43817225hg19UCSC Ensembl
Innerchr12:42102956..42103492hg18UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38537
hg19537
hg18537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418991
SamplesAK1
Known GenesADAMTS20
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)nsv819620
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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