A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17023015



Internal ID83048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:61094000..61231887hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38137888
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6141573
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17023015
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008989


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