A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560144



Internal ID333158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110907408..110922452hg38UCSC Ensembl
chr5:110243107..110258151hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3815045
hg1915045
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16973646
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560144
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