A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17024530



Internal ID84089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79712335..79712422hg38UCSC Ensembl
chr9:82327250..82327337hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487619
Supporting Variants
Samples
Known GenesTLE4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17024530
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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