A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6086n223



Internal ID22809054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:22165001..22192000hg38UCSC Ensembl
chr6:22165230..22192229hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3827000
hg1927000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6397330, nsv6414696, nsv6408672
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6086n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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