A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025676



Internal ID84853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93010487..93010615hg38UCSC Ensembl
chr9:95772769..95772897hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491934
Supporting Variants
Samples
Known GenesFGD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025676
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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