A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2680n223



Internal ID22805648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8132908..8356600hg38UCSC Ensembl
chr16:8182910..8406602hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38223693
hg19223693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6498044, nsv6496487
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2680n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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