A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6092803



Internal ID22002036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133291286..133291286hg38UCSC Ensembl
chr10:135104790..135104790hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17595161
Samples
Known GenesTUBGCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6092803
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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