A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17012971



Internal ID76323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:70499291..70516765hg38UCSC Ensembl
chr8:71411526..71429000hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3817475
hg1917475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486756
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17012971
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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