A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18272117



Internal ID20839157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89810378..89811475hg38UCSC Ensembl
chr6:90520097..90521194hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381098
hg191098
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564757
Supporting Variants
Samples
Known GenesMDN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18272117
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