A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv820213



Internal ID15584914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:228398685..228404295hg38UCSC Ensembl
Innerchr2:229263401..229269011hg19UCSC Ensembl
Innerchr2:228971645..228977255hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg385611
hg195611
hg185611
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419719
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)nsv820213
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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