A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1578n209



Internal ID22827653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68809771..68823536hg38UCSC Ensembl
chr4:69675489..69689254hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3813766
hg1913766
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5840085, nsv5840084
Samples
Known GenesUGT2B10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv1578n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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