A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5411558



Internal ID190865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22827815..22827859hg38UCSC Ensembl
chr11:22849361..22849405hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38298
hg19298
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042605
Samples
Known GenesSVIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5411558
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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