A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7813n223



Internal ID22810781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66146601..66176400hg38UCSC Ensembl
chr9:42344970..42374665hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3829800
hg1929696
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6452699, nsv6447404, nsv6445609, nsv6444423, nsv6448028
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7813n223
Frequency
Sample Size19652
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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