A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421116



Internal ID21078669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33907265..33916914hg38UCSC Ensembl
chr8:33764783..33774432hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg389650
hg199650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421116
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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