A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093711



Internal ID22002944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4735334..4735334hg38UCSC Ensembl
chr9:4735334..4735334hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17591739
Samples
Known GenesAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093711
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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