A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4750838



Internal ID20526698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1026188..1026188hg38UCSC Ensembl
chr4:1019976..1019976hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16270268
Samples
Known GenesFGFRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4750838
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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