A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664749



Internal ID21613055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:40020791..40020791hg38UCSC Ensembl
chr20:38649433..38649433hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116384
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664749
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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