A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6255294



Internal ID22059904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125432081..125432081hg38UCSC Ensembl
chr4:126353236..126353236hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17857567
Samples
Known GenesFAT4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6255294
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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