A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4771n223



Internal ID22807739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4098635..4167255hg38UCSC Ensembl
chr3:4140319..4208939hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3868621
hg1968621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6355705, nsv6363965
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4771n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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