A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4773n223



Internal ID22807741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4100085..4295563hg38UCSC Ensembl
chr3:4141769..4337247hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38195479
hg19195479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6359650, nsv6361016, nsv6361824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4773n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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