A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17733556



Internal ID157222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62229100..62229162hg38UCSC Ensembl
chr20:60804156..60804218hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5528087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17733556
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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