A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17008661



Internal ID73405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8460179..8593160hg38UCSC Ensembl
chr8:8317689..8450670hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38132982
hg19132982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479471
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17008661
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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