A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259658



Internal ID20826698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:106834923..106835446hg38UCSC Ensembl
chr3:106553770..106554293hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg38524
hg19524
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574771
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259658
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00038


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