A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257375



Internal ID20824415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:233536569..233536918hg38UCSC Ensembl
chr2:234445215..234445564hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg38350
hg19350
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6545418
Supporting Variants
Samples
Known GenesUSP40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257375
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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