A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259216



Internal ID20826256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112773280..112774005hg38UCSC Ensembl
chr3:112492127..112492852hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38726
hg19726
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6565371
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259216
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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