A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208639



Internal ID20775681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4103533..4156885hg38UCSC Ensembl
chr3:4145217..4198569hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3853353
hg1953353
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6371042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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