A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819496



Internal ID15584197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39371531..39529890hg38UCSC Ensembl
Innerchr8:39229050..39387409hg19UCSC Ensembl
Innerchr8:39348207..39506566hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38158360
hg19158360
hg18158360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418787
SamplesAK1
Known GenesADAM3A, ADAM5
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)nsv819496
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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