A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610613



Internal ID21558918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:198219797..198219797hg38UCSC Ensembl
chr3:197946668..197946668hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381537
hg191537
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17126514
SamplesHG00864
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610613
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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