A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428696



Internal ID21086249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8554289..8626518hg38UCSC Ensembl
chr8:8411799..8484028hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3872230
hg1972230
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217527
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428696
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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