A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6095036



Internal ID22004269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92428653..92428653hg38UCSC Ensembl
chr12:92822429..92822429hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597944
Samples
Known GenesCLLU1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6095036
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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