A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533960



Internal ID211271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99432924..99432924hg38UCSC Ensembl
chr3:99151768..99151768hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533960
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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