A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5610185



Internal ID21558490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:22473883..22473883hg38UCSC Ensembl
chr3:22515374..22515374hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132585
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5610185
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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