A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618459



Internal ID21810506
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 StatusS
Merged Variantsnsv6089193
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618459
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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