A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259039



Internal ID20826079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103627902..103789274hg38UCSC Ensembl
chr3:103346746..103508118hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38161373
hg19161373
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555138
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259039
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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