A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241515



Internal ID22046125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73825565..73825565hg38UCSC Ensembl
chr14:74292268..74292268hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17847843
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241515
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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