A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272866



Internal ID20482084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66805485..66805485hg38UCSC Ensembl
chr16:66839388..66839388hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4752587
Supporting Variants
Samples
Known GenesNAE1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272866
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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