A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466204



Internal ID21123757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62578446..62585970hg38UCSC Ensembl
chr11:62345918..62353442hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg387525
hg197525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993215
Samples
Known GenesTUT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466204
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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