A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264938



Internal ID20831978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165659403..165659830hg38UCSC Ensembl
chr4:166580555..166580982hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264938
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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