A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3671n223



Internal ID22806639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46453401..46459800hg38UCSC Ensembl
chr19:46956658..46963057hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6520468, nsv6530854
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3671n223
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