A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5517029



Internal ID293462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53722742..53725684hg38UCSC Ensembl
chr20:52339281..52342223hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg382943
hg192943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733073
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5517029
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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