A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2945n223



Internal ID22805913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79189087..79238100hg38UCSC Ensembl
chr16:79222984..79271997hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3849014
hg1949014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6498726, nsv6510243
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2945n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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