A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6038082



Internal ID21947425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:40247650..40247748hg38UCSC Ensembl
chr12:40641452..40641550hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17604318
Samples
Known GenesLRRK2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6038082
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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