A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064182



Internal ID21973415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110473511..110473511hg38UCSC Ensembl
chr6:110794714..110794714hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559333
Samples
Known GenesSLC22A16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064182
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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