A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662332



Internal ID21610637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110646277..110646277hg38UCSC Ensembl
chr12:111084082..111084082hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17077144
SamplesHG03125
Known GenesTCTN1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662332
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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