A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735882



Internal ID159548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140537133..140537224hg38UCSC Ensembl
chr8:141547232..141547323hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488396
Supporting Variants
Samples
Known GenesAGO2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735882
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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