A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560269



Internal ID333280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94392610..94414768hg38UCSC Ensembl
chr14:94858947..94881105hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3822159
hg1922159
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17699164
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560269
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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