A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv118n209



Internal ID22826193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:206641296..206642491hg38UCSC Ensembl
chr1:206814641..206815836hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381196
hg191196
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5829169, nsv5829170
Samples
Known GenesDYRK3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv118n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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