A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019931



Internal ID21929274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113307293..113308159hg38UCSC Ensembl
chr9:116069573..116070439hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38867
hg19867
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595635
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019931
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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