A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820158



Internal ID15238123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76627662..76629127hg38UCSC Ensembl
Innerchr17:74623744..74625209hg19UCSC Ensembl
Innerchr17:72135339..72136804hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381466
hg191466
hg181466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419264
SamplesAK1
Known GenesST6GALNAC1
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)nsv820158
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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