A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv831n209



Internal ID22826906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:36157288..36162285hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg384998
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5870162, nsv5881940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv831n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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