A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510397



Internal ID287018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132743295..132746806hg38UCSC Ensembl
chr11:132613190..132616701hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383512
hg193512
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17054516
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510397
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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