A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5523951



Internal ID300166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:22703832..22703888hg38UCSC Ensembl
chr20:22684470..22684526hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17731588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5523951
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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