A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263933



Internal ID20830973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45528938..45529539hg38UCSC Ensembl
chr3:45570430..45571031hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555054
Supporting Variants
Samples
Known GenesLARS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263933
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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