A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247544



Internal ID20814584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:16240589..16241059hg38UCSC Ensembl
chr19:16351400..16351870hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6599103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247544
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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