A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483736



Internal ID261165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59832356..59833360hg38UCSC Ensembl
chr8:60744915..60745919hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381005
hg191005
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012835
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483736
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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