A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5551437



Internal ID324894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:43073916..43073966hg38UCSC Ensembl
chr3:43115408..43115458hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16931951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5551437
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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