A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv898394



Internal ID6305405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113306765..113331532hg19UCSC Ensembl
Outerchr11:113298339..113341391hg19UCSC Ensembl
Innerchr11:112811975..112836742hg18UCSC Ensembl
Outerchr11:112803549..112846601hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1554165
SamplesMS20630
Known GenesDRD2, MIR4301
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv898394
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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