A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266995



Internal ID20834035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:69232622..69233693hg38UCSC Ensembl
chr5:68528449..68529520hg19UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg381072
hg191072
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569340
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266995
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