A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7645n223



Internal ID22810613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21301824..21319720hg38UCSC Ensembl
chr9:21301823..21319719hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3817897
hg1917897
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6426144, nsv6432607
Samples
Known GenesIFNA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7645n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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