A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626207



Internal ID21818254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53392955..53402102hg38UCSC Ensembl
chr16:53426867..53436014hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg389148
hg199148
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036647
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626207
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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