A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026227



Internal ID85223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111050494..111051137hg38UCSC Ensembl
chr9:113812774..113813417hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484969
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026227
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00281


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