A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406840



Internal ID186177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64026125..64026176hg38UCSC Ensembl
chr1:64491797..64491848hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16904216
Samples
Known GenesROR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406840
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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