A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510699



Internal ID287309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:118990758..118992771hg38UCSC Ensembl
chr11:118861468..118863481hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382014
hg192014
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052203
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510699
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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