A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5451349



Internal ID229532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25935699..26021561hg38UCSC Ensembl
chr3:25977190..26063052hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3885863
hg1985863
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16930715
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5451349
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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