A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249895



Internal ID22054505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84693242..84693242hg38UCSC Ensembl
chr15:85236473..85236473hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848731
Samples
Known GenesSEC11A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249895
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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