A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3035n223



Internal ID22806003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21420691..21711606hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38290916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6503299, nsv6498495, nsv6505232
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3035n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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