A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363378



Internal ID21020931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189593901..189598500hg38UCSC Ensembl
chr3:189311690..189316289hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212243
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363378
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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