A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv825816



Internal ID6138856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31837269..31837797hg19UCSC Ensembl
Innerchr11:31793845..31794373hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1422011
SamplesNA18997
Known GenesPAX6
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv825816
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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