A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667533



Internal ID21615838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38466686..38466686hg38UCSC Ensembl
chr20:37095329..37095329hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38338
hg19338
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116638
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667533
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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