A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510843



Internal ID287450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92766454..92766992hg38UCSC Ensembl
chr11:92499620..92500158hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38539
hg19539
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051088
Samples
Known GenesFAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510843
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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