A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522631



Internal ID298895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55434413..55441628hg38UCSC Ensembl
chr20:54050951..54058166hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg387216
hg197216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733166
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522631
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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