A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269204



Internal ID20836244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6590879..6591681hg38UCSC Ensembl
chr5:6590992..6591794hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560389
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269204
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