A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148398



Internal ID21403289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21033396..21033396hg38UCSC Ensembl
chr8:20890907..20890907hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg382489
hg192489
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634781
Supporting Variants
SamplesHG00171
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148398
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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