A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18245006



Internal ID20812046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11379546..11379936hg38UCSC Ensembl
chr19:11490222..11490612hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38391
hg19391
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599410
Supporting Variants
Samples
Known GenesEPOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18245006
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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