A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv421n206



Internal ID22755725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28050213..28054688hg38UCSC Ensembl
chr6:28017991..28022466hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg384476
hg194476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5471912, nsv5467644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv421n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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