A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7802n223



Internal ID22810770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65550301..65576000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3825700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6443560, nsv6444056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7802n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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