A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499093



Internal ID276072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79297964..79323255hg38UCSC Ensembl
chr11:79009009..79034300hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3825292
hg1925292
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048677
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499093
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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