A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17611068



Internal ID21803115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23454740..23455475hg38UCSC Ensembl
chr16:23466061..23466796hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6026334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17611068
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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