A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv368n206



Internal ID22755672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:13252762..13289803hg38UCSC Ensembl
chr4:13254386..13291427hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg3837042
hg1937042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5452895, nsv5446316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv368n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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