A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483528



Internal ID260963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11283860..11284503hg38UCSC Ensembl
chr10:11325823..11326466hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38644
hg19644
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029134
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483528
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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