A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450087



Internal ID21107640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66468595..66694615hg38UCSC Ensembl
chr10:68228353..68454373hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38226021
hg19226021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv777n223
Supporting Variantsnssv17983744
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450087
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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