A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489135



Internal ID266424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22076568..22121669hg38UCSC Ensembl
chr10:22365497..22410598hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3845102
hg1945102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033708
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489135
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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