A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4766278



Internal ID20542138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65540696..65540696hg38UCSC Ensembl
chr11:65308167..65308167hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272045
Samples
Known GenesLTBP3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4766278
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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