A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521569



Internal ID297859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33747333..33747643hg38UCSC Ensembl
chr20:32335139..32335449hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732046
Samples
Known GenesZNF341
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521569
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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