A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522874



Internal ID15103481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:9918791..10838562hg38UCSC Ensembl
Innerchr20:9899439..10819210hg19UCSC Ensembl
Innerchr20:9847439..10767210hg18UCSC Ensembl
Innerchr20:9847439..10767210hg17UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38919772
hg19919772
hg18919772
hg17919772
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698529
Samples
Known GenesANKEF1, JAG1, MIR6870, MKKS, SLX4IP, SNAP25, SNAP25-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522874
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