A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429953



Internal ID21087506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:79929506..79934498hg38UCSC Ensembl
chr8:80841741..80846733hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg384993
hg194993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171225
Samples
Known GenesMRPS28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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