A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17012326



Internal ID75888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:77858233..77892167hg38UCSC Ensembl
chr8:78770468..78804402hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3833935
hg1933935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490780
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17012326
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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