A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508352



Internal ID20881651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69009330..69099250hg38UCSC Ensembl
chr16:69043233..69133153hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3889921
hg1989921
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190536
Samples
Known GenesTANGO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508352
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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