A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819624



Internal ID15584325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:184186804..184193795hg38UCSC Ensembl
Innerchr4:185107957..185114948hg19UCSC Ensembl
Innerchr4:185344951..185351942hg18UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg386992
hg196992
hg186992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1419800
SamplesAK1
Known GenesENPP6
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)nsv819624
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