A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031118



Internal ID88449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134254549..134280813hg38UCSC Ensembl
chr9:137146395..137172659hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3826265
hg1926265
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489539
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031118
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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