A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819879



Internal ID15237844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:64508426..64508655hg38UCSC Ensembl
Innerchr17:62504544..62504773hg19UCSC Ensembl
Innerchr17:59935006..59935235hg18UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38230
hg19230
hg18230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419337
SamplesAK1
Known GenesCEP95
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)nsv819879
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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