A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486291



Internal ID263660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59302541..59303644hg38UCSC Ensembl
chr8:60215100..60216203hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17012800
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486291
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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