A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4768n223



Internal ID22807736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4066144..4176829hg38UCSC Ensembl
chr3:4107828..4218513hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38110686
hg19110686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6374486, nsv6370762
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4768n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer