A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv787n209



Internal ID22826862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3653625..3670359hg38UCSC Ensembl
chr16:3703626..3720360hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3816735
hg1916735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5937513, nsv5932725
Samples
Known GenesDNASE1, TRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv787n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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