A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497730



Internal ID274754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96588182..96594364hg38UCSC Ensembl
chr11:96459182..96465364hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386183
hg196183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052152
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497730
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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