A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261757



Internal ID20828797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:119967950..119969200hg38UCSC Ensembl
chr3:119686797..119688047hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg381251
hg191251
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561565
Supporting Variants
Samples
Known GenesGSK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261757
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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