A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596677



Internal ID20969748
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 StatusM
Merged Variants
Supporting Variantsnssv18244989
Samples
Known GenesC19orf38, DNM2, MIR199A1, MIR4748, MIR6793, TMED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596677
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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