A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5651740



Internal ID21600045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35861691..35861691hg38UCSC Ensembl
chr13:36435828..36435828hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085593
SamplesNA20509
Known GenesDCLK1, MIR548F5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5651740
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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