A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521016



Internal ID297322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:44848963..44855927hg38UCSC Ensembl
chr20:43477604..43484568hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg386965
hg196965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732578
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521016
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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