A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545206



Internal ID21869561
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 StatusS
Merged Variantsnsv6079805
Supporting Variants
Samples
Known GenesRICTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545206
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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