A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561480



Internal ID334459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96952374..96972352hg38UCSC Ensembl
chr15:97495604..97515582hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3819979
hg1919979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17705575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561480
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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