A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3926793



Internal ID21346863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28267076..28267076hg38UCSC Ensembl
chr8:28124593..28124593hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg38344
hg19344
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204406
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3926793
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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