A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522690



Internal ID15103297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:33427230..33552481hg38UCSC Ensembl
Innerchr20:32015036..32140287hg19UCSC Ensembl
Innerchr20:31478697..31603948hg18UCSC Ensembl
Innerchr20:31478697..31603948hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38125252
hg19125252
hg18125252
hg17125252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706100
Samples
Known GenesCBFA2T2, SNTA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522690
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