A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563164



Internal ID336101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58731684..58731699hg38UCSC Ensembl
chr20:57306740..57306755hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38487
hg19487
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563164
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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