A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508184



Internal ID284880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134867822..134946364hg38UCSC Ensembl
chr11:134737716..134816258hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3878543
hg1978543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053851
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508184
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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