A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358671



Internal ID21016224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172519242..172568656hg38UCSC Ensembl
chr3:172237032..172286446hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3849415
hg1949415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209222
Samples
Known GenesTNFSF10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358671
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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