A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv878667



Internal ID6285678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9551094..9901563hg19UCSC Ensembl
Outerchr4:9543673..9903121hg19UCSC Ensembl
Innerchr4:9160192..9510661hg18UCSC Ensembl
Outerchr4:9152771..9512219hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1547770
SamplesMS17537
Known GenesDRD5, MIR548I2, SLC2A9
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv878667
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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