A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523597



Internal ID299823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40098520..40103973hg38UCSC Ensembl
chr20:38727161..38732614hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg385454
hg195454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523597
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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