A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638028



Internal ID21586333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92895782..92895782hg38UCSC Ensembl
chr8:93908010..93908010hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17158294
SamplesNA20509
Known GenesTRIQK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638028
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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