A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17010448



Internal ID74589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25648246..25659394hg38UCSC Ensembl
chr8:25505762..25516910hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3811149
hg1911149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476234
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17010448
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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