A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656366



Internal ID21604671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81426354..81426354hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381046
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090254
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656366
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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