A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483691



Internal ID261124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22276943..22290811hg38UCSC Ensembl
chr10:22565872..22579740hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3813869
hg1913869
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033726
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483691
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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