A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097408



Internal ID22006641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132539067..132539067hg38UCSC Ensembl
chr9:135414454..135414454hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597289
Samples
Known GenesC9orf171
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097408
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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