A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096926



Internal ID22006159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:320804..320804hg38UCSC Ensembl
chr9:320804..320804hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17580402
Samples
Known GenesDOCK8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096926
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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