A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5477526



Internal ID255104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108620240..108621779hg38UCSC Ensembl
chr8:109632469..109634008hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg381540
hg191540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015138
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5477526
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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