A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819662



Internal ID15584363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:49203187..49210312hg38UCSC Ensembl
Innerchr8:50115746..50122871hg19UCSC Ensembl
Innerchr8:50278299..50285424hg18UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg387126
hg197126
hg187126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419807
SamplesAK1
Known Genes
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)nsv819662
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer