A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17116554



Internal ID21452086
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 StatusS
Merged Variantsnsv5671455
Supporting Variants
SamplesHG01596
Known GenesDYNLRB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17116554
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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