A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17013119



Internal ID76418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75134057..75139293hg38UCSC Ensembl
chr8:76046292..76051528hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg385237
hg195237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5489792
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17013119
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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