A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2203n209



Internal ID22828278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130263902..130268169hg38UCSC Ensembl
chr9:133026181..133030448hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg384268
hg194268
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5858720, nsv5857291
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2203n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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