A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020459



Internal ID21929802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35494895..35546726hg38UCSC Ensembl
chr9:35494892..35546723hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3851832
hg1951832
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584993
Samples
Known GenesRUSC2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020459
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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