A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2108n209



Internal ID22828183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40229279..43206180hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382976902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5909117, nsv5911060
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2108n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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