A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6241651



Internal ID22046261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:88026379..88026379hg38UCSC Ensembl
chr14:88492723..88492723hg19UCSC Ensembl
Cytoband14q31.3
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 Variantsnssv17846391
Samples
Known GenesLINC01146
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6241651
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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