A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249866



Internal ID22054476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81067730..81067730hg38UCSC Ensembl
chr15:81360071..81360071hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848699
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249866
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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