A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937513



Internal ID22712882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3653883..3670359hg38UCSC Ensembl
chr16:3703884..3720360hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3816477
hg1916477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv787n209
Supporting Variantsnssv17386911
Samples
Known GenesDNASE1, TRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937513
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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