A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421086



Internal ID200174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64355251..64355302hg38UCSC Ensembl
chr15:64647450..64647501hg19UCSC Ensembl
Cytoband15q22.31
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 Variantsnssv17704190
Samples
Known GenesCSNK1G1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421086
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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