A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7669n223



Internal ID22810637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28348168..28591853hg38UCSC Ensembl
chr9:28348166..28591851hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38243686
hg19243686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6435081, nsv6422571
Samples
Known GenesLINGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7669n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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