A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505313



Internal ID282094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95196935..95197013hg38UCSC Ensembl
chr11:94930099..94930177hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050042
Samples
Known GenesSESN3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505313
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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