A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7809n223



Internal ID22810777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65707801..65725500hg38UCSC Ensembl
chr9:42688721..42706420hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3817700
hg1917700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6440832, nsv6438297
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7809n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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