A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946102



Internal ID22721587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59392910..59393019hg38UCSC Ensembl
chr16:59426814..59426923hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387919
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946102
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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