A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671455



Internal ID21619760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34523917..34523917hg38UCSC Ensembl
chr20:33111722..33111722hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg381346
hg191346
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116554
SamplesHG01596
Known GenesDYNLRB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671455
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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