A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069135



Internal ID21978368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83145204..83145204hg38UCSC Ensembl
chr6:83854923..83854923hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568270
Samples
Known GenesDOPEY1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069135
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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