A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758499



Internal ID20534359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69301180..69301180hg38UCSC Ensembl
chr11:69068647..69068647hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758499
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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