A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014051



Internal ID21923394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13325125..13345244hg38UCSC Ensembl
chr9:13325124..13345243hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3820120
hg1920120
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17578942
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014051
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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