A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010009



Internal ID74313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:26420790..26422844hg38UCSC Ensembl
chr8:26278306..26280360hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg382055
hg192055
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486431
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010009
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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