A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18242153



Internal ID20809193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35580277..35582083hg38UCSC Ensembl
chr17:33907296..33909102hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381807
hg191807
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582281
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18242153
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