A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1899n223



Internal ID22804867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68397538..68625443hg38UCSC Ensembl
chr13:68971670..69199575hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38227906
hg19227906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6490174, nsv6483951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv1899n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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