A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262828



Internal ID20829868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49478354..49479068hg38UCSC Ensembl
chr3:49515787..49516501hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550447
Supporting Variants
Samples
Known GenesDAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262828
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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