A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4766n223



Internal ID22807734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4009545..4114078hg38UCSC Ensembl
chr3:4051229..4155762hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38104534
hg19104534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6358763, nsv6360842
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv4766n223
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