A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv218n206



Internal ID22755522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32077980..32085995hg38UCSC Ensembl
chr17:30404999..30413014hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg388016
hg198016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6144420, nsv6145255
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv218n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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