A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559813



Internal ID332836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67561844..67581790hg38UCSC Ensembl
chr10:69321602..69341548hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3819947
hg1919947
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037334
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559813
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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