A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2808n223



Internal ID22805776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34188201..34221200hg38UCSC Ensembl
chr16:33990668..34023150hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3833000
hg1932483
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6497446, nsv6501931, nsv6510034, nsv6514244, nsv6508761
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2808n223
Frequency
Sample Size19652
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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