A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7768n223



Internal ID22810736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63544101..63644300hg38UCSC Ensembl
chr9:68139835..68240034hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38100200
hg19100200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6440987, nsv6445837
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7768n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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