A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18241617



Internal ID20808657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28021306..28021956hg38UCSC Ensembl
chr17:26348332..26348982hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38651
hg19651
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6588019
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18241617
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