A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092212



Internal ID22001445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64896492..64896492hg38UCSC Ensembl
chr16:64930395..64930395hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17620295
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092212
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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