A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5518436



Internal ID294824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33770848..33777339hg38UCSC Ensembl
chr20:32358654..32365145hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg386492
hg196492
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732048
Samples
Known GenesZNF341
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5518436
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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