A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424036



Internal ID21081589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79982170..79982462hg38UCSC Ensembl
chr8:80894405..80894697hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227621
Samples
Known GenesMRPS28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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