A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465205



Internal ID21122758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66743901..66745800hg38UCSC Ensembl
chr11:66511372..66513271hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190620
Samples
Known GenesC11orf80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465205
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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