A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560441



Internal ID333448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63545829..63566397hg38UCSC Ensembl
chr14:64012547..64033115hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3820569
hg1920569
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560441
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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