A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028799



Internal ID86909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128425157..128433195hg38UCSC Ensembl
chr9:131187436..131195474hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg388039
hg198039
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558902
Supporting Variants
Samples
Known GenesCERCAM
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028799
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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