A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2689n223



Internal ID22805657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11457364..11537099hg38UCSC Ensembl
chr16:11551220..11630955hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3879736
hg1979736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6507785, nsv6506674
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2689n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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