A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6460846



Internal ID21118399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107408159..107408717hg38UCSC Ensembl
chr11:107278885..107279443hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38559
hg19559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17986538
Samples
Known GenesCWF19L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6460846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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