A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089193



Internal ID21998426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85991553..85991553hg38UCSC Ensembl
chr16:86025159..86025159hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17618459
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089193
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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