A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6041n223



Internal ID22809009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:458438..866903hg38UCSC Ensembl
chr6:458438..866903hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38408466
hg19408466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6413804, nsv6398391
Samples
Known GenesEXOC2, HUS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6041n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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