A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5580516



Internal ID21529007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11494..11773hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17130900
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5580516
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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