A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819933



Internal ID15584634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55703444..55704292hg38UCSC Ensembl
Innerchr16:55737356..55738204hg19UCSC Ensembl
Innerchr16:54294857..54295705hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38849
hg19849
hg18849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419101
SamplesAK1
Known GenesSLC6A2
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)nsv819933
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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