A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040465



Internal ID94684
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 StatusS
Merged Variantsnsv5561233
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040465
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer