A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18216566



Internal ID20783606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106944462..106945621hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6615909
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18216566
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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