A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244549



Internal ID20811589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72315311..72338511hg38UCSC Ensembl
chr17:70311452..70334652hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3823201
hg1923201
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588451
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244549
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