A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016355



Internal ID21925698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116798613..116826759hg38UCSC Ensembl
chr9:119560892..119589038hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3828147
hg1928147
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597208
Samples
Known GenesASTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016355
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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