A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209341



Internal ID20776381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4864701..4871000hg38UCSC Ensembl
chr3:4906385..4912684hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372231
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209341
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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