A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656278



Internal ID21604583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110839119..110839119hg38UCSC Ensembl
chr13:111491466..111491466hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17088634
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656278
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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