A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260465



Internal ID22065075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:68460841..68460841hg38UCSC Ensembl
chr5:67756668..67756668hg19UCSC Ensembl
Cytoband5q13.1
Allele length
AssemblyAllele length
hg38213
hg19213
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17857752
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260465
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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