A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5435296



Internal ID213947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99275000..99289574hg38UCSC Ensembl
chr3:98993844..99008418hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3814575
hg1914575
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16937398
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5435296
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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