A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7686n223



Internal ID22810654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32079901..32091800hg38UCSC Ensembl
chr9:32079899..32091798hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3811900
hg1911900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6433681, nsv6428901
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7686n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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