A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557824



Internal ID330910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223854721..223855233hg38UCSC Ensembl
chr2:224719438..224719950hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16923965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557824
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