A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113305



Internal ID21296571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:21534456..21539935hg38UCSC Ensembl
Innerchr20:21515094..21520573hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg385480
hg195480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14100836
Samplessample417
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113305
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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