A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2961n223



Internal ID22805929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89753944..89866045hg38UCSC Ensembl
chr16:89820352..89932453hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38112102
hg19112102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6502305, nsv6496303, nsv6512901
Samples
Known GenesFANCA, SPIRE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2961n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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