A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097977



Internal ID22007210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133391278..133391278hg38UCSC Ensembl
chr9:136257054..136257054hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17587837
Samples
Known GenesC9orf96
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6097977
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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