A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17028167



Internal ID86474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:130363851..130363909hg38UCSC Ensembl
chr9:133239238..133239296hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479877
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17028167
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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