A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17052602



Internal ID102925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:114638519..114675752hg38UCSC Ensembl
chr11:114509241..114546474hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3837234
hg1937234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497168
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17052602
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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