A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519490



Internal ID15446783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26244015..26328619hg38UCSC Ensembl
Innerchr20:26224651..26309255hg19UCSC Ensembl
Innerchr20:26172651..26257255hg18UCSC Ensembl
Innerchr20:26172651..26257255hg17UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg3884605
hg1984605
hg1884605
hg1784605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv658126, nssv656460, nssv662535, nssv656401, nssv658882, nssv687870, nssv687215, nssv662169, nssv675939, nssv693910, nssv661412, nssv691264, nssv677451, nssv675506
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519490
Frequency
Sample Size2026
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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