A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084148



Internal ID21993381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:111326328..111326328hg38UCSC Ensembl
chr12:111764132..111764132hg19UCSC Ensembl
Cytoband12q24.12
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606147
Samples
Known GenesCUX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084148
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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