A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208963



Internal ID20776003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13168926..13200021hg38UCSC Ensembl
chr3:13210426..13241521hg19UCSC Ensembl
Cytoband3p25.2
Allele length
AssemblyAllele length
hg3831096
hg1931096
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208963
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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