A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671819



Internal ID21620127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37743951..37743951hg38UCSC Ensembl
chr20:36372353..36372353hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116220
SamplesHG00171
Known GenesCTNNBL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671819
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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