A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247539



Internal ID20814579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16155821..16156314hg38UCSC Ensembl
chr19:16266631..16267124hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599794
Supporting Variants
Samples
Known GenesHSH2D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247539
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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