A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026871



Internal ID21936214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10008..19656hg38UCSC Ensembl
chr16:60008..69656hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389649
hg199649
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603761
Samples
Known GenesDDX11L10, MIR6859-1, MIR6859-2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026871
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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