A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533712



Internal ID309596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33737470..33744730hg38UCSC Ensembl
chr20:32325276..32332536hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg387261
hg197261
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17732045
Samples
Known GenesZNF341
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533712
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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