A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026695



Internal ID85527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109139110..109143189hg38UCSC Ensembl
chr9:111901390..111905469hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg384080
hg194080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487457
Supporting Variants
Samples
Known GenesFRRS1L
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026695
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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