A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv308n206



Internal ID22755612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14870138..15194801hg38UCSC Ensembl
chr20:14850784..15175447hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38324664
hg19324664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5521929, nsv5522032
Samples
Known GenesMACROD2, MACROD2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)dgv308n206
Frequency
Sample Size3202
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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