A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425902



Internal ID204853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24822702..24822753hg38UCSC Ensembl
chr14:25291908..25291959hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693462
Samples
Known GenesSTXBP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425902
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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