A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281149



Internal ID20848189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81510262..81511082hg38UCSC Ensembl
chr9:84125177..84125997hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg38821
hg19821
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558319
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281149
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