A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244989



Internal ID20812029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10733096..10849613hg38UCSC Ensembl
chr19:10843772..10960289hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38116518
hg19116518
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596677
Supporting Variants
Samples
Known GenesC19orf38, DNM2, MIR199A1, MIR4748, MIR6793, TMED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244989
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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