A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7811n223



Internal ID22810779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66145201..66203500hg38UCSC Ensembl
chr9:42317743..42376065hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3858300
hg1958323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6438651, nsv6449444, nsv6442398
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7811n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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