A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv895371



Internal ID6302382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49494478..50222585hg19UCSC Ensembl
Outerchr10:49492075..50232180hg19UCSC Ensembl
Innerchr10:49164484..49892591hg18UCSC Ensembl
Outerchr10:49162081..49902186hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1521079
SamplesSP51402
Known GenesARHGAP22, LRRC18, MAPK8, MIR4294, VSTM4, WDFY4
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv895371
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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