A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4761431



Internal ID20537291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129889661..129889661hg38UCSC Ensembl
chr11:129759556..129759556hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16269166
Samples
Known GenesNFRKB
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4761431
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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