A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418241



Internal ID21075794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86652313..86662914hg38UCSC Ensembl
chr8:87664541..87675142hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3810602
hg1910602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229230
Samples
Known GenesCNGB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418241
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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