A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6533825



Internal ID20907186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3956712..3957959hg38UCSC Ensembl
chr19:3956710..3957957hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381248
hg191248
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18198128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6533825
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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