A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17158294



Internal ID21508540
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 StatusS
Merged Variantsnsv5638028
Supporting Variants
SamplesNA20509
Known GenesTRIQK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17158294
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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