A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646208



Internal ID21594513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109694251..109694251hg38UCSC Ensembl
chr13:110346598..110346598hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17080635
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646208
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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