A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406669



Internal ID186008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26317695..26317746hg38UCSC Ensembl
chr1:26644186..26644237hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16902453
Samples
Known GenesUBXN11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406669
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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