A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406854



Internal ID186191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95096526..95096577hg38UCSC Ensembl
chr11:94829690..94829741hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38251
hg19251
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050034
Samples
Known GenesENDOD1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406854
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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