A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv441n209



Internal ID22826516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93457770..93461463hg38UCSC Ensembl
chr12:93851546..93855239hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg383694
hg193694
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5856894, nsv5848631
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv441n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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