A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020683



Internal ID21930026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68221743..68222004hg38UCSC Ensembl
chr15:68514081..68514342hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617045
Samples
Known GenesCLN6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020683
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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