A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496192



Internal ID20869391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:52472458..52519873hg38UCSC Ensembl
chr16:52506370..52553785hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3847416
hg1947416
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192366
Samples
Known GenesTOX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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