A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428886



Internal ID21086439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33382692..33462940hg38UCSC Ensembl
chr8:33240210..33320458hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3880249
hg1980249
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225338
Samples
Known GenesFUT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428886
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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