A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419080



Internal ID21076633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79925835..79926643hg38UCSC Ensembl
chr8:80838070..80838878hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171224
Samples
Known GenesMRPS28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419080
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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