A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2811n223



Internal ID22805779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34215801..34267700hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3851900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6498616, nsv6499686, nsv6504712, nsv6505770, nsv6505748, nsv6515163, nsv6504938, nsv6511619, nsv6501556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2811n223
Frequency
Sample Size19652
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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