A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17147457



Internal ID21404833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:19865786..19865786hg38UCSC Ensembl
chr8:19723297..19723297hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5638239
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17147457
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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