A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5665151



Internal ID21613456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:17880281..17880281hg38UCSC Ensembl
chr20:17860925..17860925hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg386056
hg196056
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115789
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5665151
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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