A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249793



Internal ID22054403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69508528..69508528hg38UCSC Ensembl
chr15:69800867..69800867hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38263
hg19263
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17846897
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249793
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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