A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089108



Internal ID21998341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132378604..132378604hg38UCSC Ensembl
chr9:135253991..135253991hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17582257
Samples
Known GenesTTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089108
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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