A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17622938



Internal ID21814985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49379459..49379459hg38UCSC Ensembl
chr16:49413370..49413370hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6095022
Supporting Variants
Samples
Known GenesC16orf78
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17622938
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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