A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688356



Internal ID112022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29399580..29419595hg38UCSC Ensembl
chr11:29421127..29441142hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3820016
hg1920016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5505460
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688356
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000625


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