A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7806n223



Internal ID22810774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65698901..65718500hg38UCSC Ensembl
chr9:42679821..42699420hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3819600
hg1919600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6442056, nsv6443688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7806n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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