A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441923



Internal ID220370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148893013..148898254hg38UCSC Ensembl
chr3:148610800..148616041hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg385242
hg195242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16940793
Samples
Known GenesCPA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441923
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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