A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6084557



Internal ID21993790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40298860..40298860hg38UCSC Ensembl
chr12:40692662..40692662hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617026
Samples
Known GenesLRRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6084557
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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