A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261163



Internal ID20828203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179690721..179691111hg38UCSC Ensembl
chr3:179408509..179408899hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557451
Supporting Variants
Samples
Known GenesUSP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261163
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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