A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5516586



Internal ID293038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:39721093..39726768hg38UCSC Ensembl
chr20:38349735..38355410hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg385676
hg195676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5516586
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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