A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079805



Internal ID21989038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:38982523..38982523hg38UCSC Ensembl
chr5:38982625..38982625hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17545206
Samples
Known GenesRICTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079805
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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