A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240115



Internal ID22044725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109027251..109027251hg38UCSC Ensembl
chr9:111789531..111789531hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17841289
Samples
Known GenesTMEM245
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240115
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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