A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516426



Internal ID6015775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:101479975..101497921hg19UCSC Ensembl
Innerchr15:99297498..99315444hg18UCSC Ensembl
Innerchr15:99297498..99315444hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnssv656567, nssv692347, nssv668291, nssv702318
Samples
Known GenesLRRK1
Method
AnalysisMerged-level CNV regions
PlatformIllumina HumanHap550 Genotyping BeadChip v3
Comments
ReferenceShaikh et al 2009
Pubmed ID19592680
Accession Number(s)nsv516426
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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