A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5418803



Internal ID197960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23906305..23906367hg38UCSC Ensembl
chr1:24232795..24232857hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901131
Samples
Known GenesCNR2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5418803
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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