A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609842



Internal ID21801889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:83417854..83419781hg38UCSC Ensembl
chr12:83811633..83813560hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg381928
hg191928
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6029381
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609842
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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