A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483179



Internal ID260621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21742843..21752707hg38UCSC Ensembl
chr10:22031772..22041636hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg389865
hg199865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17033682
Samples
Known GenesMLLT10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483179
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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