A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552113



Internal ID21876468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1812531..1812531hg38UCSC Ensembl
chr5:1812645..1812645hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6066984
Supporting Variants
Samples
Known GenesNDUFS6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552113
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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