A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024063



Internal ID21933406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3706461..3707185hg38UCSC Ensembl
chr16:3756462..3757186hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17607750
Samples
Known GenesTRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024063
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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