A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18247600



Internal ID20814640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18212736..18213272hg38UCSC Ensembl
chr19:18323546..18324082hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6595939
Supporting Variants
Samples
Known GenesPDE4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18247600
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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