A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2n206



Internal ID22755306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:523968..531968hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg388001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6138828, nsv6138820
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv2n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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