A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269611



Internal ID20836651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74934364..74938318hg38UCSC Ensembl
chr5:74230189..74234143hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg383955
hg193955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563504
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269611
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