A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv825755



Internal ID6138795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6613228..6677844hg19UCSC Ensembl
Innerchr11:6569804..6634420hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1439111
SamplesNA18973
Known GenesDCHS1, ILK, RRP8, TAF10, TPP1
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv825755
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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