A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17051674



Internal ID102291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128700440..128713490hg38UCSC Ensembl
chr11:128570335..128583385hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3813051
hg1913051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496641
Supporting Variants
Samples
Known GenesFLI1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17051674
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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