A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5584146



Internal ID21532681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108752945..108753534hg38UCSC Ensembl
chr3:108471792..108472381hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17135682
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5584146
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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