A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4962n223



Internal ID22807930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:103389001..103415100hg38UCSC Ensembl
chr3:103107845..103133944hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3826100
hg1926100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6374946, nsv6372047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4962n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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