A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv872535



Internal ID6279546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:169536650..169538603hg19UCSC Ensembl
Outerchr1:169535918..169538842hg19UCSC Ensembl
Innerchr1:167803274..167805227hg18UCSC Ensembl
Outerchr1:167802542..167805466hg18UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1504703
SamplesSP52708
Known GenesF5
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv872535
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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