A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260413



Internal ID20827453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155823318..155824040hg38UCSC Ensembl
chr3:155541107..155541829hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573841
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260413
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00029


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