A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044815



Internal ID97625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:20883122..21568664hg38UCSC Ensembl
chr11:20904668..21590210hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38685543
hg19685543
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496577
Supporting Variants
Samples
Known GenesNELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044815
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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