A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249859



Internal ID22054469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80270144..80270144hg38UCSC Ensembl
chr15:80562486..80562486hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848692
Samples
Known GenesLINC00927
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249859
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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