A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5528367



Internal ID304426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:21828280..21829244hg38UCSC Ensembl
chr20:21808918..21809882hg19UCSC Ensembl
Cytoband20p11.22
Allele length
AssemblyAllele length
hg38965
hg19965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731551
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5528367
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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