A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216787



Internal ID20783827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108521418..108568632hg38UCSC Ensembl
chr6:108842621..108889835hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3847215
hg1947215
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604845
Supporting Variants
Samples
Known GenesFOXO3, LACE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216787
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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