A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441786



Internal ID220238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25410804..25412430hg38UCSC Ensembl
chr3:25452295..25453921hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg381627
hg191627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931314
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441786
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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