A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2082n209



Internal ID22828157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:20958299..20969149hg38UCSC Ensembl
chr9:20958298..20969148hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3810851
hg1910851
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5861531, nsv5852287
Samples
Known GenesFOCAD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2082n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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