A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2083n209



Internal ID22828158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21193534..21214402hg38UCSC Ensembl
chr9:21193533..21214401hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3820869
hg1920869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5920674, nsv5916420
Samples
Known GenesIFNA10, IFNA7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2083n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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