A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516591



Internal ID15443884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16257378..16267808hg38UCSC Ensembl
Innerchr20:16238023..16248453hg19UCSC Ensembl
Innerchr20:16186023..16196453hg18UCSC Ensembl
Innerchr20:16186023..16196453hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3810431
hg1910431
hg1810431
hg1710431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv244n21
Supporting Variantsnssv669435, nssv657049, nssv658558
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516591
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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