A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261799



Internal ID20828839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121617457..121618423hg38UCSC Ensembl
chr3:121336304..121337270hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38967
hg19967
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564625
Supporting Variants
Samples
Known GenesFBXO40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261799
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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