A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066651



Internal ID21975884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:165618985..165618985hg38UCSC Ensembl
chr6:166032473..166032473hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558375
Samples
Known GenesPDE10A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066651
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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