A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516018



Internal ID15096625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:32596479..32667182hg38UCSC Ensembl
Innerchr20:31184281..31254984hg19UCSC Ensembl
Innerchr20:30647942..30718645hg18UCSC Ensembl
Innerchr20:30647942..30718645hg17UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg3870704
hg1970704
hg1870704
hg1770704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663676, nssv702315, nssv652419
Samples
Known GenesC20orf203, LOC149950
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516018
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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