A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028825



Internal ID86928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128666636..128668182hg38UCSC Ensembl
chr9:131428915..131430461hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381547
hg191547
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563589
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028825
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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