A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954420



Internal ID21374490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:128726820..128726820hg38UCSC Ensembl
chr8:129739066..129739066hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg383404
hg193404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15204686
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954420
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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