A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486365



Internal ID263735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11054460..11153277hg38UCSC Ensembl
chr10:11096423..11195240hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3898818
hg1998818
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17059077
Samples
Known GenesCELF2, CELF2-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486365
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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