A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666834



Internal ID21615142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62166667..62166667hg38UCSC Ensembl
chr20:60741723..60741723hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117597
SamplesHG00512
Known GenesSS18L1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666834
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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