A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5520556



Internal ID296881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19748495..19749301hg38UCSC Ensembl
chr20:19729139..19729945hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38807
hg19807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731428
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5520556
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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