A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4865n223



Internal ID22807833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48129355..48149105hg38UCSC Ensembl
chr3:48170845..48190595hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3819751
hg1919751
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6365482, nsv6366032
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4865n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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