A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854580



Internal ID22038223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:108066178..108066178hg38UCSC Ensembl
chr4:108987334..108987334hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255123
Supporting Variants
Samples
Known GenesLEF1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854580
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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