A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026269



Internal ID85250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111491574..111493475hg38UCSC Ensembl
chr9:114253854..114255755hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg381902
hg191902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026269
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002342


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