A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18281313



Internal ID20848353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86572177..86572809hg38UCSC Ensembl
chr9:89187092..89187724hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18281313
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00017


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