A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5397494



Internal ID176900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95203161..95203212hg38UCSC Ensembl
chr11:94936325..94936376hg19UCSC 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 Variantsnssv17050044
Samples
Known GenesSESN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5397494
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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