A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17854591



Internal ID22038234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109000850..109000850hg38UCSC Ensembl
chr4:109922006..109922006hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6255134
Supporting Variants
Samples
Known GenesCOL25A1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17854591
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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