A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5407194



Internal ID186529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53395097..53395148hg38UCSC Ensembl
chr4:54261264..54261315hg19UCSC Ensembl
Cytoband4q12
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 Variantsnssv16951042
Samples
Known GenesFIP1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5407194
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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