A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2100n209



Internal ID22828175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33423085..33424832hg38UCSC Ensembl
chr9:33423083..33424830hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381748
hg191748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5919628, nsv5921417
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2100n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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