A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256411



Internal ID22061021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:166012104..166012104hg38UCSC Ensembl
chr5:165439109..165439109hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17858813
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256411
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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