A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv369n206



Internal ID22755673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16726452..16726506hg38UCSC Ensembl
chr4:16728075..16728129hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5409365, nsv5407923
Samples
Known GenesLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv369n206
Frequency
Sample Size3202
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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