A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512093



Internal ID288661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:23835630..23887345hg38UCSC Ensembl
chr11:23857176..23908891hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3851716
hg1951716
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512093
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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