A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv879536



Internal ID6286547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:90687507..90765280hg19UCSC Ensembl
Outerchr4:90678541..90775212hg19UCSC Ensembl
Innerchr4:90906530..90984303hg18UCSC Ensembl
Outerchr4:90897564..90994235hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1594954
SamplesIS40067
Known GenesSNCA
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv879536
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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