A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv859n209



Internal ID22826934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:139394..143030hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5885905, nsv5885283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv859n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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