A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260260



Internal ID22064870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43393704..43393704hg38UCSC Ensembl
chr5:43393806..43393806hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17857177
Samples
Known GenesCCL28
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260260
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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