A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418261



Internal ID21075814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79987754..80008752hg38UCSC Ensembl
chr8:80899989..80920987hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3820999
hg1920999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229117
Samples
Known GenesMRPS28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418261
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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