A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262675



Internal ID20829715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:46508518..46509302hg38UCSC Ensembl
chr3:46550008..46550792hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546158
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262675
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00053


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