A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17610142



Internal ID21802189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40247729..40247729hg38UCSC Ensembl
chr12:40641531..40641531hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092273
Supporting Variants
Samples
Known GenesLRRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17610142
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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