A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522290



Internal ID20895651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12692449..12707347hg38UCSC Ensembl
chr19:12803263..12818161hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3814899
hg1914899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197357
Samples
Known GenesFBXW9, SNORD41, TNPO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522290
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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