A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060706



Internal ID21969939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41914475..41914475hg38UCSC Ensembl
chr5:41914577..41914577hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17549474
Samples
Known GenesC5orf51
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060706
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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