A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513766



Internal ID290281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43328904..43328954hg38UCSC Ensembl
chr11:43350454..43350504hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044018
Samples
Known GenesAPI5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513766
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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