A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2006n209



Internal ID22828081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:36408724..36411643hg38UCSC Ensembl
chr8:36266242..36269161hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382920
hg192920
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5853634, nsv5854496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2006n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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