A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522347



Internal ID298618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59148399..59148723hg38UCSC Ensembl
chr20:57723454..57723778hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733366
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522347
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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