A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451789



Internal ID229959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:114642581..114642709hg38UCSC Ensembl
chr3:114361428..114361556hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936427
Samples
Known GenesZBTB20
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451789
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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