A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6242067



Internal ID22046677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51866568..51866568hg38UCSC Ensembl
chr15:52158765..52158765hg19UCSC Ensembl
Cytoband15q21.2
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 Variantsnssv17846615
Samples
Known GenesTMOD3
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6242067
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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