A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089041



Internal ID21998274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:107716795..107716795hg38UCSC Ensembl
chr9:110479076..110479076hg19UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg38168
hg19168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17585780
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089041
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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