A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465034



Internal ID21122587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116149701..116151900hg38UCSC Ensembl
chr11:116020418..116022617hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1319n223
Supporting Variantsnssv18189666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465034
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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