A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450924



Internal ID229117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:113157755..113175003hg38UCSC Ensembl
chr3:112876602..112893850hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3817249
hg1917249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16938360
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450924
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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