A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6093111



Internal ID22002344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40314034..40314034hg38UCSC Ensembl
chr9:42459052..42459052hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596277
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6093111
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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