A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509471



Internal ID286122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:126912686..126912816hg38UCSC Ensembl
chr11:126782582..126782712hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17688457
Samples
Known GenesKIRREL3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509471
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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