A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520563



Internal ID15447856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63687658..63688119hg38UCSC Ensembl
Innerchr3:63673334..63673795hg19UCSC Ensembl
Innerchr3:63648374..63648835hg18UCSC Ensembl
Innerchr3:63648374..63648835hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38462
hg19462
hg18462
hg17462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677342, nssv672555
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520563
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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