A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17014507



Internal ID77341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93855609..93857822hg38UCSC Ensembl
chr8:94867837..94870050hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382214
hg192214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488550
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17014507
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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