A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7732n223



Internal ID22810700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41265401..41364900hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3899500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6454868, nsv6441312, nsv6445169, nsv6454772
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7732n223
Frequency
Sample Size19652
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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