A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5581673



Internal ID21530176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:170682057..170682107hg38UCSC Ensembl
chr3:170399846..170399896hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17132209
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5581673
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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