A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561233



Internal ID334218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123721967..123735105hg38UCSC Ensembl
chr10:125481483..125494621hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3813139
hg1913139
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040465
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561233
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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