A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279676



Internal ID20846716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:115565097..115568269hg38UCSC Ensembl
chr9:118327376..118330548hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg383173
hg193173
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279676
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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