A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv894911



Internal ID6301922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:17061681..17080633hg19UCSC Ensembl
Outerchr10:17059462..17081139hg19UCSC Ensembl
Innerchr10:17101687..17120639hg18UCSC Ensembl
Outerchr10:17099468..17121145hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1579672
SamplesIS35148
Known GenesCUBN
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv894911
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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