A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259193



Internal ID20826233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:111583786..111588198hg38UCSC Ensembl
chr3:111302633..111307045hg19UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg384413
hg194413
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567315
Supporting Variants
Samples
Known GenesCD96
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259193
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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