A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895736



Internal ID6302747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79742617..79904144hg19UCSC Ensembl
Outerchr10:79740262..79914190hg19UCSC Ensembl
Innerchr10:79412623..79574150hg18UCSC Ensembl
Outerchr10:79410268..79584196hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1526887
SamplesSP57950
Known GenesPOLR3A, RPS24
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895736
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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