A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17008691



Internal ID73425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9165262..9165931hg38UCSC Ensembl
chr8:9022772..9023441hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38670
hg19670
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478961
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17008691
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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