A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434488



Internal ID213161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48387184..48387409hg38UCSC Ensembl
chr3:48428675..48428900hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16932704
Samples
Known GenesFBXW12
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434488
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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