A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5448959



Internal ID227211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46508758..46509326hg38UCSC Ensembl
chr3:46550248..46550816hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16933309
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5448959
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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