A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819165



Internal ID15237130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:95247287..95248635hg38UCSC Ensembl
Innerchr8:96259515..96260863hg19UCSC Ensembl
Innerchr8:96328691..96330039hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg381349
hg191349
hg181349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419242
SamplesAK1
Known GenesC8orf37
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)nsv819165
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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