A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428422



Internal ID21085975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:124771691..124780323hg38UCSC Ensembl
chr8:125783933..125792565hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg388633
hg198633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18164083
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428422
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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