A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262568



Internal ID20829608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148761373..148781731hg38UCSC Ensembl
chr3:148479160..148499518hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3820359
hg1920359
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556849
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262568
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.06437


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