A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5543299



Internal ID204002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184826152..184826155hg38UCSC Ensembl
chr4:185747306..185747309hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5543299
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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