A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4674n223



Internal ID22807642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28194464..28213500hg38UCSC Ensembl
chr22:28590452..28609488hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3819037
hg1919037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6538337, nsv6537555
Samples
Known GenesTTC28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4674n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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