A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17008232



Internal ID73117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8630894..8633448hg38UCSC Ensembl
chr8:8488404..8490958hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg382555
hg192555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481899
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17008232
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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