A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422413



Internal ID21079966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:28486488..28487523hg38UCSC Ensembl
chr8:28344005..28345040hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg381036
hg191036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166154
Samples
Known GenesFBXO16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422413
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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