A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039254



Internal ID93896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115135083..115152775hg38UCSC Ensembl
chr10:116894846..116912540hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3817693
hg1917695
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6147382
Supporting Variants
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039254
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.003279


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