A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660874



Internal ID21609179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35350843..35350843hg38UCSC Ensembl
chr19:35841746..35841746hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38812
hg19812
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17104298
SamplesHG00096
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660874
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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