A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2026n209



Internal ID22828101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108514400..108522548hg38UCSC Ensembl
chr8:109526629..109534777hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg388149
hg198149
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5858790, nsv5848591
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2026n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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