A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030110



Internal ID87792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133620684..133621584hg38UCSC Ensembl
chr9:136485806..136486706hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476860
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030110
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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