A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7814n223



Internal ID22810782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66146701..66157000hg38UCSC Ensembl
chr9:42364335..42374565hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3810300
hg1910231
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6452036, nsv6440691, nsv6449508, nsv6436312
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7814n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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