A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023586



Internal ID83439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33974298..34176660hg38UCSC Ensembl
chr9:33974296..34176658hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38202363
hg19202363
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142143
Supporting Variants
Samples
Known GenesDCAF12, UBAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023586
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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