A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5661284



Internal ID21609589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:92428637..92428637hg38UCSC Ensembl
chr12:92822413..92822413hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087279
SamplesHG00731
Known GenesCLLU1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5661284
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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