A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904146



Internal ID6266073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43309429..43403955hg19UCSC Ensembl
Outerchr15:43294218..43414673hg19UCSC Ensembl
Innerchr15:41096721..41191247hg18UCSC Ensembl
Outerchr15:41081510..41201965hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1584754
SamplesIS37167
Known GenesUBR1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904146
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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