A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501534



Internal ID278430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:65928947..65931135hg38UCSC Ensembl
chr14:66395665..66397853hg19UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg382189
hg192189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698189
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501534
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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