A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263327



Internal ID20830367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177485474..177489723hg38UCSC Ensembl
chr3:177203262..177207511hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg384250
hg194250
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574941
Supporting Variants
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263327
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