A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369506



Internal ID21027059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109746704..110087812hg38UCSC Ensembl
chr3:109465551..109806659hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38341109
hg19341109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207229
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369506
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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