A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245687



Internal ID20812727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46686645..46688622hg38UCSC Ensembl
chr19:47189902..47191879hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg381978
hg191978
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6597339
Supporting Variants
Samples
Known GenesPRKD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245687
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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