A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028079



Internal ID86416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129365065..129374259hg38UCSC Ensembl
chr9:132127344..132136538hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg389195
hg199195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028079
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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