A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670289



Internal ID21618596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64105811..64105811hg38UCSC Ensembl
chr20:62737164..62737164hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117806
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670289
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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