A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17012787



Internal ID76196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:57910060..57910125hg38UCSC Ensembl
chr8:58822619..58822684hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476485
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17012787
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.028255


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