A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024496



Internal ID84065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79186475..79186544hg38UCSC Ensembl
chr9:81801390..81801459hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480612
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024496
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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