A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7798n223



Internal ID22810766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65474201..65515700hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3841500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6449225, nsv6437079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7798n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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