A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518119



Internal ID15445412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31950507..31956217hg38UCSC Ensembl
Innerchr21:33322819..33328529hg19UCSC Ensembl
Innerchr21:32244690..32250400hg18UCSC Ensembl
Innerchr21:32244690..32250400hg17UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg385711
hg195711
hg185711
hg175711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695536
Samples
Known GenesHUNK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518119
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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