A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv904147



Internal ID6266074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43319431..43392075hg19UCSC Ensembl
Outerchr15:43309429..43403955hg19UCSC Ensembl
Innerchr15:41106723..41179367hg18UCSC Ensembl
Outerchr15:41096721..41191247hg18UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1568796
SamplesIS31338
Known GenesUBR1
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv904147
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer