A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4974n223



Internal ID22807942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108755301..109297541hg38UCSC Ensembl
chr3:108474148..109016388hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38542241
hg19542241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6372551, nsv6365771
Samples
Known GenesDPPA2, FLJ22763, GUCA1C, LINC00488, MORC1, RETNLB, TRAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4974n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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