A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264087



Internal ID20831127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94377512..94377832hg38UCSC Ensembl
chr3:94096356..94096676hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264087
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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