A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506716



Internal ID283453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33867780..33867863hg38UCSC Ensembl
chr11:33889326..33889409hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044135
Samples
Known GenesLMO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506716
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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