A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7529n223



Internal ID22810497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144916067..144923864hg38UCSC Ensembl
chr8:146141452..146149250hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg387798
hg197799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6422409, nsv6435302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7529n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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