A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5522185



Internal ID298458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:35201826..35202616hg38UCSC Ensembl
chr20:33789629..33790419hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38791
hg19791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5522185
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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