A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4953n223



Internal ID22807921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:100610201..100726500hg38UCSC Ensembl
chr3:100329045..100445344hg19UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38116300
hg19116300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6363972, nsv6357858
Samples
Known GenesGPR128, TFG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4953n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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