A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6096773



Internal ID22006006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94621398..94621398hg38UCSC Ensembl
chr9:97383680..97383680hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17596708
Samples
Known GenesFBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6096773
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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