A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028788



Internal ID86899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128290809..128290886hg38UCSC Ensembl
chr9:131053088..131053165hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5482962
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028788
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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