A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv826091



Internal ID6139131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113929116..113933766hg19UCSC Ensembl
Innerchr11:113434326..113438976hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1433080
SamplesNA18972
Known GenesZBTB16
Method
AnalysisIdentical to variant call (no regions submitted)
PlatformAgilent 24M aCGH
Comments
ReferencePark_et_al_2010
Pubmed ID20364138
Accession Number(s)nsv826091
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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