A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516426



Internal ID8410701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:100939770..100957716hg38UCSC Ensembl
Innerchr15:101479975..101497921hg19UCSC Ensembl
Innerchr15:99297498..99315444hg18UCSC Ensembl
Innerchr15:99297498..99315444hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3817947
hg1917947
hg1817947
hg1717947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv656567, nssv692347, nssv668291, nssv702318
Samples
Known GenesLRRK1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
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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