A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579556



Internal ID21771599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18646593..18656289hg38UCSC Ensembl
chr10:18935522..18945218hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg389697
hg199697
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015319
Supporting Variants
Samples
Known GenesNSUN6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579556
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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