A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv841n209



Internal ID22826916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47181912..47186764hg38UCSC Ensembl
chr16:47215823..47220675hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg384853
hg194853
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5884387, nsv5878055
Samples
Known GenesITFG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv841n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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