A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18254520



Internal ID20821560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145858541..145858982hg38UCSC Ensembl
chr2:146616109..146616550hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38442
hg19442
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541470
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18254520
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