A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460458



Internal ID238440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109778997..109800019hg38UCSC Ensembl
chr4:110700153..110721175hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3821023
hg1921023
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954903
Samples
Known GenesCFI
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460458
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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