A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7679n223



Internal ID22810647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:30045471..30165905hg38UCSC Ensembl
chr9:30045469..30165903hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38120435
hg19120435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6427316, nsv6435020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7679n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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