A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv826911



Internal ID6139951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:29238303..29238789hg19UCSC Ensembl
Innerchr14:28308054..28308540hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1439952
SamplesNA18537
Known GenesFOXG1
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv826911
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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