A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009451



Internal ID73936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33385582..33389923hg38UCSC Ensembl
chr8:33243100..33247441hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg384342
hg194342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493535
Supporting Variants
Samples
Known GenesFUT10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009451
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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