A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433756



Internal ID212459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114319024..114319075hg38UCSC Ensembl
chr11:114189746..114189797hg19UCSC Ensembl
Cytoband11q23.2
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 Variantsnssv17052525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5433756
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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