A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260816



Internal ID20470034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86120796..86120796hg38UCSC Ensembl
chr16:86154402..86154402hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260816
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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