A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv419n206



Internal ID22755723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6984112..6984162hg38UCSC Ensembl
chr6:6984345..6984395hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5551852, nsv5541019
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv419n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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