A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538566



Internal ID313637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94621373..94621406hg38UCSC Ensembl
chr11:94354539..94354572hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17049995
Samples
Known GenesPIWIL4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538566
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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