A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5668793



Internal ID21617098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:50782523..50803563hg38UCSC Ensembl
chr19:51285780..51306820hg19UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3821041
hg1921041
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17105653
Samples
Known GenesACPT, C19orf48, SNORD88A, SNORD88B, SNORD88C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5668793
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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