A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv442n206



Internal ID22755746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16000..28000hg38UCSC Ensembl
chr7:16000..28000hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3812001
hg1912001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6141727, nsv6142684
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv442n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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