A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261162



Internal ID20828202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179690619..179691005hg38UCSC Ensembl
chr3:179408407..179408793hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567637
Supporting Variants
Samples
Known GenesUSP13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261162
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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