A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940473



Internal ID21360542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:21416005..21416328hg38UCSC Ensembl
chr3:21457497..21457820hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179167
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940473
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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