A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151415



Internal ID21495108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92492289..92492289hg38UCSC Ensembl
chr8:93504517..93504517hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625069
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151415
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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