A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7859n223



Internal ID22810827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82754601..82773323hg38UCSC Ensembl
chr9:85369516..85388238hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3818723
hg1918723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6439529, nsv6451747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7859n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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