A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221902



Internal ID20788942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41974172..41975311hg38UCSC Ensembl
chr13:42548308..42549447hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6593490
Supporting Variants
Samples
Known GenesVWA8-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221902
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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