A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6064067



Internal ID21973300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3385821..3385821hg38UCSC Ensembl
chr6:3386055..3386055hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382046
hg192046
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559502
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6064067
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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