A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088854



Internal ID21998087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:13599474..13599474hg38UCSC Ensembl
chr16:13693331..13693331hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603391
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088854
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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