A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17053263



Internal ID103362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121857205..121872624hg38UCSC Ensembl
chr11:121727913..121743332hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3815420
hg1915420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497777
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17053263
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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