A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506678



Internal ID283418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35047975..35049992hg38UCSC Ensembl
chr11:35069522..35071539hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382018
hg192018
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044187
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506678
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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