A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360634



Internal ID21018187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39775101..39782100hg38UCSC Ensembl
chr3:39816592..39823591hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211209
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360634
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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