A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3279n223



Internal ID22806247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10606001..10607800hg38UCSC Ensembl
chr18:10605998..10607797hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6521496, nsv6523781
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3279n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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