A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819930



Internal ID8551620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:79598775..79599795hg38UCSC Ensembl
Innerchr16:79632672..79633692hg19UCSC Ensembl
Innerchr16:78190173..78191193hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg381021
hg191021
hg181021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419153
SamplesAK1
Known GenesMAF
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)nsv819930
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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