A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560172



Internal ID333186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162042488..162052885hg38UCSC Ensembl
chr1:162012278..162022675hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3810398
hg1910398
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16892449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560172
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