A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013477



Internal ID76659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86405393..86406770hg38UCSC Ensembl
chr8:87417622..87418999hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381378
hg191378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485620
Supporting Variants
Samples
Known GenesWWP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013477
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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