A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819809



Internal ID15237774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:66803132..66810460hg38UCSC Ensembl
Innerchr16:66837035..66844363hg19UCSC Ensembl
Innerchr16:65394536..65401864hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg387329
hg197329
hg187329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419823
SamplesAK1
Known GenesNAE1
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)nsv819809
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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