A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554271



Internal ID327465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73368322..73368507hg38UCSC Ensembl
chr14:73835030..73835215hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698286
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554271
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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