A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7395n223



Internal ID22810363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79178711..79267380hg38UCSC Ensembl
chr8:80090946..80179615hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3888670
hg1988670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6429655, nsv6431261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7395n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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