A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031219



Internal ID88513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135000118..135009387hg38UCSC Ensembl
chr9:137891964..137901233hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg389270
hg199270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475703
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031219
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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