A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495466



Internal ID272579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108469074..108470675hg38UCSC Ensembl
chr11:108339801..108341402hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381602
hg191602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495466
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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