A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506658



Internal ID283398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44655351..44656719hg38UCSC Ensembl
chr11:44676901..44678269hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381369
hg191369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046136
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506658
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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